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Haplogroup P (Y-DNA)
Human Y-chromosome DNA haplogroup
Human Y-chromosome DNA haplogroup
| Field | Value |
|---|---|
| name | P (K2b2) |
| map | Haplogroup P of Y-DNA.png |
| origin-date | 44,000 to 41,000 years BP |
| origin-place | South Asia, or Southeast Asia |
| ancestor | PF5850 within K2b |
| descendants | P-M45 (P1~, formerly P1, a.k.a. QR) and others |
| mutations | P295/PF5866/S8, 92R7_1, 92R7_2, F91/PF5862/V231 |
| origin-date = 44,000 to 41,000 years BP | origin-place = South Asia, or Southeast Asia
Haplogroup P also known as P-P295 or K2b2 is a Y-chromosome DNA haplogroup in human genetics, it forms a clade within Haplogroup K2b (K-P331). Its sister clade within K2b is K2b1 (haplogroup MS).
It was proposed to redefine the root of Haplogroup P through the novel Single-nucleotide polymorphism PF5850, yet this is so far not reflected in the International Society of Genetic Genealogy Y-DNA Haplogroup Tree nor in scientific publications.
Basal PF5850* is found in Southeast Asia. Basal P-P295* is found among South and Southeast Asians as well as Oceanians, P-FT292000 (P1b, formerly P3) with unknown distribution, and P-M45* (P1~*) commonly found among Siberians and Central Asians. P-M45 is the parent node of Haplogroup Q (Q-M242) and Haplogroup R (R-M207).
The major subclades of Haplogroups P-M45, Q and R now include most males among Europeans, Native Americans, South Asians, North Africans, and Central Asians.
Origin and dispersal

Karafet et al. 2015 suggests an origin and dispersal of haplogroup P and its ancestral clade K from either South Asia or Southeast Asia as part of the early human dispersal, based on the distribution of subclades of P-P295 and more ancient clades such as K1 and K2. However, Karafet, et al. mentions that this hypothesis is "parsimonious" and K may have alternatively originated elsewhere in Eurasia and later went extinct there. According to a geneticist Spencer Wells, haplogroup K, from which haplogroup P descended, originated most likely in the Middle East or Central Asia. According to Bergstorm et al (2016), haplogroup K2b1 (Y-haplogroup S/M) found in Indigenous Australians and ancestors of haplogroup R and Q (Y-haplogroup K2b2/root P) split in Southeast Asia near Sahul.
The highest frequency and diversity of haplogroup P clades is observed in Southeast Asia, specifically on the Malay Peninsula and the Philippines. To date, the ancestral clade K2b has only been confirmed among the 39,000 year old Tianyuan man.
Structure
Main article: Structure of Y-DNA Haplogroup K
The subclades of Haplogroup P with their defining mutation(s):
K2b
- PF5850
- P (P295/PF5866/S8, PF5870/F115/M1189/V1651)
- P1 (CTS196/PF5845, ...)
- P1~ (M45/PF5962, P226/PF5879, ...)
- Q (M242, F4052/M1063/V1090, ...)
- R (P224, P227, P229, P232, P280, P285, L248.3/M705.3, ...)
- P2 (F20148, ...)
- P2a~ (B253/Z33760/Z33761/Z33762/Z33763)
- P2b (F24883)
- P2b1 (BY49600/Y145258, ...)
- P (P295/PF5866/S8, PF5870/F115/M1189/V1651)
Distribution
PF5850*
PF5850* was found among a Jehai sample in Malaysia. Basal P1* was also found in one historical 19th-century Andaman islander.
P*(xP1~)
This paraphyletic group comprises all subclades of P-P295 except for the main clade P-M45 (thus also excludes haplogroups Q and R). The position of P1~ alias P-M45 within P is not confirmed, thus the tilde suffix. Because P2 (P-F20148) was discovered relatively recently, it is not always clear if older studies have screened for it. Therefore, cases reported as P-P295* or K2b2* in older literature likely include P-B253.
P*(xP1~) exists at low to moderate levels among various groups in Island South East Asia, the South West Pacific and East Asia.
P*(xP1~) is found at its highest rate among members of the Aeta (or Agta), a people indigenous to Luzon who formed from various ancient groups, such as Oceanians and Austronesian peoples from Taiwan. P1*(xQ,R) is most common among individuals in Siberia and Central Asia, as well as in Southern Asian at lower frequency.
| Population | P* % | Notes |
|---|---|---|
| Papua New Guinea | 0.69 | assumed from Kayser et al. 2006 1 P* found |
| New Zealand | 0 | |
| Fiji | 0 | |
| Solomon Islands | 0 | |
| French Polynesia | 0 | |
| Vanuatu | 0 | |
| New Caledonia | ||
| Guam | 0 | |
| Samoa | 0 | |
| Kiribati | ||
| Tonga | 0 | |
| Micronesia FDR | 0 | |
| Marshall Islands | 0 | |
| American Samoa | ||
| Northern Mariana Islands | ||
| Palau | ||
| Cook Islands | 0 | |
| Wallis and Futuna | 0 | |
| Tuvalu | 0 | |
| Nauru | ||
| Norfolk Island | ||
| Niue | 0 | small sample size |
| Tokelau | 0 | small sample size |
| Hawaii | 0 | small sample size from FTDNA |
| Australia | 0 | |
| Timor | 10.8 | |
| Aeta (Philippines) | 28 | |
| Austronesians (Philippines) | 0 | |
| Malaysia | 0 | |
| Flores | 0 | |
| Sulawesi | 0.6 | |
| East Indonesia | 0 | |
| Java Indonesia | 0 | |
| Bali Indonesia | 0 | |
| Sumatra Indonesia | 0 | |
| Borneo Indonesia | 0 | |
| West Papua Province | 0 | |
| Papua Province | 0 | |
| Sumba Indonesia | 3.2 |
P-M45 (P1~)
Derived P1~ (P-M45) has been found among the Ancient North Eurasian Yana specimens, which carried around 29–47% ancestry from an East Eurasian source represented by the Tianyuan man.
Many modern ethnic groups with high frequencies of P1~, also known as P-M45 and K2b2a, are located in Central Asia and Siberia: 35.4% among Tuvans, 28.3% among Altai-Kizhi (PxQ-M3,R1), and 35% among Nivkh males.
| Modern population | Modern ethnolinguistic affiliation | Reference | n | Percentage | Notes/SNPs tested | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Tuvinian | ||||||||||
| Nivkh | ||||||||||
| Altai-Kizhi | ||||||||||
| Todjin | ||||||||||
| Chukchi | ||||||||||
| Koryak | ||||||||||
| Yupik | ||||||||||
| Uighur | ||||||||||
| Kalmyk | ||||||||||
| Turkmen | ||||||||||
| Soyot | ||||||||||
| Uriankhai | ||||||||||
| Khakas | ||||||||||
| Kazakh | ||||||||||
| Uzbek | ||||||||||
| Khasi-Khmuic | ||||||||||
| Munda | ||||||||||
| Nicobarese | ||||||||||
| Southeast Asia | ||||||||||
| Garo | ||||||||||
| India | ||||||||||
| East Asia | ||||||||||
| Eastern India | ||||||||||
| Southern Talysh, Iran | ||||||||||
| Northern Talysh, Azerbaijan | ||||||||||
| Mazandarani | ||||||||||
| Gilaki | ||||||||||
| Tehran | ||||||||||
| Isfahan | ||||||||||
| Bakhtiari | ||||||||||
| Iranian Arabs | ||||||||||
| North Iran | ||||||||||
| South Iran | ||||||||||
| South Caucacus | ||||||||||
| South Caucacus | ||||||||||
| Hvar | ||||||||||
| Korčula |
§ May include members of haplogroup R2.
| Population group | N | P (xQ, xR) | Q | R | Count | % | Count | % | Count | % |
|---|---|---|---|---|---|---|---|---|---|---|
| Gope | 16 | 1 | 6.4 | |||||||
| Oriya Brahmin | 24 | 1 | 4.2 | |||||||
| Mahishya | 17 | 3 | 17.6 | |||||||
| Bhumij | 15 | 2 | 13.3 | |||||||
| Saora | 13 | 3 | 23.1 | |||||||
| Nepali | 7 | 2 | 28.6 | |||||||
| Muslims of Manipur | 9 | 3 | 33.3 | |||||||
| Himachal Pradesh Rajput | 15 | 1 | 6.7 | |||||||
| Lambadi | 18 | 4 | 22.2 | |||||||
| Gujarati Patel | 9 | 2 | 22.2 | |||||||
| Katkari | 19 | 1 | 5.3 | |||||||
| Madia Gond | 14 | 1 | 7.1 | |||||||
| Kamma Chowdary | 15 | 0 | 0 | 1 | 6.7 | 12 | 80 |
Q
Near universal in the Kets (95%) of Siberia. Very common in pre-modern Native American populations and Selkups, except for the Na-Dene peoples, where it reaches 50-90%. Also common, at 25-50% in Siberian populations such as the Siberian Tatars, Nivkh, Tuvans, Chukchi, Siberian Eskimos, Northern Altaians, and in 70% of Turkmens.
R
The only discovered case of basal R* (i.e. one that does not belong to R1 or R2) is the Mal'ta Boy in the Upper Paleolithic on the upper Angara River in the area west of Lake Baikal in the Irkutsk Oblast, Siberia, Russian Federation.
R1
| Continental | Country | Population | Sample | R1a1 | R1a1* | R1a1a | Source | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Caucasus | Ossetians | North | 134 | NA | 0.00 | 0.75 | vauthors = Underhill PA, Myres NM, Rootsi S, Metspalu M, Zhivotovsky LA, King RJ, Lin AA, Chow CE, Semino O, Battaglia V, Kutuev I, Järve M, Chaubey G, Ayub Q, Mohyuddin A, Mehdi SQ, Sengupta S, Rogaev EI, Khusnutdinova EK, Pshenichnov A, Balanovsky O, Balanovska E, Jeran N, Augustin DH, Baldovic M, Herrera RJ, Thangaraj K, Singh V, Singh L, Majumder P, Rudan P, Primorac D, Villems R, Kivisild T | title = Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a | journal = European Journal of Human Genetics | volume = 18 | issue = 4 | pages = 479–484 | date = April 2010 | pmid = 19888303 | doi = 10.1038/ejhg.2009.194 | pmc = 2987245 | ref = | publication-date = April 2010 }} | ||
| Europe | Estonia | 100 | NA | 0.00 | 35.00 | |||||||||||||||
| Europe | Romania | 335 | NA | 0.00 | 17.01 | |||||||||||||||
| Europe | Croatia | Krk (island) | 74 | NA | 0.00 | 36.49 | ||||||||||||||
| Europe | Croatia | Brac (island) | 49 | NA | 0.00 | 24.49 | ||||||||||||||
| Europe | Croatia | Hvar (island) | 91 | NA | 0.00 | 6.59 | ||||||||||||||
| Europe | Croatia | Korcula (island) | 134 | NA | 0.00 | 15.67 | ||||||||||||||
| Europe | Croatia | mainland | 108 | NA | 0.00 | 26.85 | ||||||||||||||
| Europe | Bosnia-Herzegovina | Herzegovina | 141 | NA | 0.00 | 12.06 | ||||||||||||||
| Europe | Kosovo | Albanians | 114 | NA | 0.00 | 3.51 | ||||||||||||||
| Europe | Serbia | 113 | NA | 0.00 | 18.58 | |||||||||||||||
| Europe | Republic of Macedonia | Macedonia | 79 | NA | 0.00 | 13.92 | ||||||||||||||
| Europe | Czech Republic | 53 | NA | 0.00 | 37.74 | |||||||||||||||
| Europe | Belarus | Brest | 97 | NA | 0.00 | 58.8 | vauthors = Underhill PA, Poznik GD, Rootsi S, Järve M, Lin AA, Wang J, Passarelli B, Kanbar J, Myres NM, King RJ, Di Cristofaro J, Sahakyan H, Behar DM, Kushniarevich A, Sarac J, Saric T, Rudan P, Pathak AK, Chaubey G, Grugni V, Semino O, Yepiskoposyan L, Bahmanimehr A, Farjadian S, Balanovsky O, Khusnutdinova EK, Herrera RJ, Chiaroni J, Bustamante CD, Quake SR, Kivisild T, Villems R | title = The phylogenetic and geographic structure of Y-chromosome haplogroup R1a | journal = European Journal of Human Genetics | volume = 23 | issue = 1 | pages = 124–131 | date = January 2015 | pmid = 24667786 | doi = 10.1038/ejhg.2014.50 | pmc = 4266736 | ref = }} | |||
| Europe | Belarus | 267 | NA | 0.00 | 54.7 | |||||||||||||||
| Europe | Belarus | 50 | NA | 0.00 | 42.00 | |||||||||||||||
| Europe | Russia | Russians | 39 | NA | 0.00 | 38.46 | ||||||||||||||
| Central Asia | Tajiks, Turkmens | 38 | NA | 0.00 | 7.89 | |||||||||||||||
| North Asia | Russia | Tuvas | 104 | NA | 0.00 | 7.69 | ||||||||||||||
| North Asia | Russia | Altaians | 58 | NA | 0.00 | 41.38 | ||||||||||||||
| South Asia | India | Jammu Jharkhand | 61 | NA | 0.00 | 37.70 | ||||||||||||||
| South Asia | India | Andhra-Pradesh Jharkhand | 19 | NA | 0.00 | 26.32 | ||||||||||||||
| South Asia | India | Madhya-Pradesh Madhya-Pradesh | 54 | NA | 0.00 | 35.19 | ||||||||||||||
| South Asia | India | Khatri-Punjab/Haryana | 15 | NA | 0.00 | 67.00 | ||||||||||||||
| South Asia | India | Ahir-Punjab/Haryana | 24 | NA | 0.00 | 63.00 | ||||||||||||||
| South Asia | India | Uttar-Pradesh Jharkhand | 171 | NA | 0.00 | 49.71 | ||||||||||||||
| South Asia | India | Uttranchal Jharkhand | 21 | NA | 0.00 | 47.62 | ||||||||||||||
| South Asia | India | West-Bengal Chhattisgarh | 49 | NA | 0.00 | 48.98 | ||||||||||||||
| South Asia | India | Asur Maharashtra | 88 | NA | 0.00 | 5.68 | ||||||||||||||
| South Asia | India | Ho Madhya-Pradesh | 45 | NA | 0.00 | 0.00 | ||||||||||||||
| South Asia | India | Mawasi Orissa | 27 | NA | 0.00 | 3.70 | ||||||||||||||
| South Asia | India | Mawasi Chhattisgarh | 12 | NA | 0.00 | 8.33 | ||||||||||||||
| South Asia | India | Mahali Orissa | 32 | NA | 0.00 | 9.38 | ||||||||||||||
| South Asia | India | Santhal Meghalaya | 20 | NA | 0.00 | 10.00 | ||||||||||||||
| South Asia | India | Birhor Meghalaya | 27 | NA | 0.00 | 3.70 | ||||||||||||||
| South Asia | India | Birhor | 35 | NA | 0.00 | 2.86 | ||||||||||||||
| South Asia | India | Baiga | 23 | NA | 0.00 | 8.70 | ||||||||||||||
| South Asia | India | Baiga | 42 | NA | 0.00 | 2.38 | ||||||||||||||
| South Asia | India | Kharia | 37 | NA | 0.00 | 5.41 | ||||||||||||||
| South Asia | India | Savara | 21 | NA | 0.00 | 9.52 | ||||||||||||||
| South Asia | India | Meghwal Rajasthan | 50 | NA | 0.00 | 30.00 | ||||||||||||||
| South Asia | India | Garo | 25 | NA | 0.00 | 4.00 | ||||||||||||||
| South Asia | India | Lohana Gujarat | 20 | NA | 0.00 | 60.00 | ||||||||||||||
| South Asia | India | Khasi | 21 | NA | 0.00 | 4.76 | ||||||||||||||
| South Asia | Iran | 87 | NA | 0.00 | 10.34 | |||||||||||||||
| South Asia | Pakistan | Sindhi | 134 | NA | 0.00 | 49.00 | ||||||||||||||
| South Asia | Pakistan | Mohanna | 70 | NA | 0.00 | 71.00 | ||||||||||||||
| Europe | Turkey | 89 | NA | 0.00 | 3.37 | |||||||||||||||
| Caucasus | Armenia | 25 | NA | 0.00 | 4.00 | |||||||||||||||
| Caucasus | Megrels | 67 | NA | 0.00 | 8.96 | |||||||||||||||
| Caucasus | Abkhazes | 162 | NA | 0.00 | 9.26 | |||||||||||||||
| Caucasus | Avars | 42 | NA | 0.00 | 2.38 | |||||||||||||||
| Caucasus | Chamalals | 27 | NA | 0.00 | 7.41 | |||||||||||||||
| Caucasus | Bagvalals | 28 | NA | 0.00 | 3.57 | |||||||||||||||
| Caucasus | Andis | 49 | NA | 0.00 | 2.04 | |||||||||||||||
| Caucasus | Lezgis | 31 | NA | 0.00 | 0.00 | |||||||||||||||
| Caucasus | Darginians | 68 | NA | 0.00 | 0.00 | |||||||||||||||
| Caucasus | Tabasarans | 43 | NA | 0.00 | 2.33 | |||||||||||||||
| Caucasus | Adyghes | 160 | NA | 0.00 | 11.25 | |||||||||||||||
| Caucasus | Karachays | 69 | NA | 0.00 | 27.54 | |||||||||||||||
| Caucasus | Kumyks | 76 | NA | 0.00 | 13.16 | |||||||||||||||
| Caucasus | Balkars | 136 | NA | 0.00 | 25.74 | |||||||||||||||
| Caucasus | Cherkessians | 126 | NA | 0.00 | 12.70 | |||||||||||||||
| Caucasus | Kabardians | 141 | NA | 0.71 | 13.48 | |||||||||||||||
| Caucasus | Abazas | 89 | NA | 0.00 | 19.10 | |||||||||||||||
| Caucasus | Nogays | 87 | NA | 0.00 | 12.64 | |||||||||||||||
| Caucasus | Karanogays | 77 | NA | 0.00 | 9.09 | |||||||||||||||
| Caucasus | Tats | 10 | NA | 0.00 | 0.00 | |||||||||||||||
| Europe | Crete | 193 | NA | 0.00 | 8.81 | |||||||||||||||
| Middle East | Oman | 121 | NA | 0.00 | 9.09 | |||||||||||||||
| Middle East | Iran | 150 | NA | 0.67 | 12.67 | |||||||||||||||
| Middle East | United Arab Emirates | 164 | NA | 0.00 | 7.32 | |||||||||||||||
| Europe | Turkey | 523 | NA | 0.00 | 6.88 | |||||||||||||||
| Europe | Lithuania | Aukštaičiai | 106 | 45.3 | NA | NA | vauthors = Kasperaviciūte D, Kucinskas V, Stoneking M | title = Y chromosome and mitochondrial DNA variation in Lithuanians | journal = Annals of Human Genetics | volume = 68 | issue = Pt 5 | pages = 438–452 | date = September 2004 | pmid = 15469421 | doi = 10.1046/j.1529-8817.2003.00119.x | ref = | s2cid = 26562505 | orig-date = online September 2004 }} | ||
| Europe | Lithuania | Žemaičiai | 90 | 44.4 | NA | NA | ||||||||||||||
| Europe | Norway | North | 377 | 27.1 | NA | NA | vauthors = Dupuy BM, Stenersen M, Lu TT, Olaisen B | title = Geographical heterogeneity of Y-chromosomal lineages in Norway | journal = Forensic Science International | volume = 164 | issue = 1 | pages = 10–19 | date = December 2006 | pmid = 16337760 | doi = 10.1016/j.forsciint.2005.11.009 | ref = }} | ||||
| Europe | Norway | Middle | 317 | 31.5 | NA | NA | ||||||||||||||
| Europe | Norway | West | 301 | 24.3 | NA | NA | ||||||||||||||
| Europe | Norway | East | 493 | 26.8 | NA | NA | ||||||||||||||
| Europe | Norway | Bergen | 93 | 28 | NA | NA | ||||||||||||||
| Europe | Norway | Oslo | 109 | 19.3 | NA | NA | ||||||||||||||
| Europe | Norway | South | 76 | 13.2 | NA | NA | ||||||||||||||
| Europe | Spain/Portugal | large survey | 1140 | NA | 0.00 | 1.2 | vauthors = Adams SM, Bosch E, Balaresque PL, Ballereau SJ, Lee AC, Arroyo E, López-Parra AM, Aler M, Grifo MS, Brion M, Carracedo A, Lavinha J, Martínez-Jarreta B, Quintana-Murci L, Picornell A, Ramon M, Skorecki K, Behar DM, Calafell F, Jobling MA | title = The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula | journal = American Journal of Human Genetics | volume = 83 | issue = 6 | pages = 725–736 | date = December 2008 | pmid = 19061982 | pmc = 2668061 | doi = 10.1016/j.ajhg.2008.11.007 | ref = }} | |||
| Europe | Greece | Greeks | 92 | NA | 0.00 | 16.3 | vauthors = Battaglia V, Fornarino S, Al-Zahery N, Olivieri A, Pala M, Myres NM, King RJ, Rootsi S, Marjanovic D, Primorac D, Hadziselimovic R, Vidovic S, Drobnic K, Durmishi N, Torroni A, Santachiara-Benerecetti AS, Underhill PA, Semino O | title = Y-chromosomal evidence of the cultural diffusion of agriculture in Southeast Europe | journal = European Journal of Human Genetics | volume = 17 | issue = 6 | pages = 820–830 | date = June 2009 | pmid = 19107149 | pmc = 2947100 | doi = 10.1038/ejhg.2008.249 | ref = | orig-date = online December 2008 }} | ||
| Europe | Greece | Macedonian Greeks | 57 | NA | 1.80 | 10.5 | ||||||||||||||
| Europe | Albania | 55 | NA | 0.00 | 9.1 | |||||||||||||||
| Europe | Bosnia | Serbs | 81 | NA | 0.00 | 13.6 | ||||||||||||||
| Europe | Bosnia | Bosniacs | 84 | NA | 0.00 | 15.5 | ||||||||||||||
| Europe | Bosnia | Croats | 90 | NA | 0.00 | 12.2 | ||||||||||||||
| Europe | Croatia | 89 | NA | 0.00 | 27.0 | |||||||||||||||
| Europe | Hungary | 53 | NA | 0.00 | 56.6 | |||||||||||||||
| Europe | Czech Republic | 75 | NA | 0.00 | 41.3 | |||||||||||||||
| Europe | Poland | 99 | NA | 0.00 | 56.6 | |||||||||||||||
| Europe | Ukraine | 92 | NA | 0.00 | 50.0 | |||||||||||||||
| Europe | Georgia | 66 | NA | 0.00 | 10.6 | |||||||||||||||
| Europe | Russia | Balkarians | 38 | NA | 0.00 | 13.2 | ||||||||||||||
| Europe | Republic of Macedonia | Albanian language | 64 | NA | 0.00 | 1.6 | ||||||||||||||
| Europe | Croatia | Osijek | 29 | NA | 0.00 | 37.9 | ||||||||||||||
| Europe | Slovenia | Slovenians | 75 | NA | 0.00 | 38.70 | ||||||||||||||
| Europe | Italy | North East | 67 | NA | 0.00 | 10.4 | ||||||||||||||
| - | - | Ashkenazi Cohen | 76 | NA | 0.00 | 1.3 | vauthors = Behar DM, Thomas MG, Skorecki K, Hammer MF, Bulygina E, Rosengarten D, Jones AL, Held K, Moses V, Goldstein D, Bradman N, Weale ME | title = Multiple origins of Ashkenazi Levites: Y chromosome evidence for both Near Eastern and European ancestries | journal = American Journal of Human Genetics | volume = 73 | issue = 4 | pages = 768–779 | date = October 2003 | pmid = 13680527 | pmc = 1180600 | doi = 10.1086/378506 }} | ||||
| - | - | Sephardi Cohen | 69 | NA | 0.00 | 5.8 | ||||||||||||||
| Europe | - | Ashkenazi Levite | 60 | NA | 0.00 | 51.7 | ||||||||||||||
| - | - | Sephardi Levite | 31 | NA | 0.00 | 3.2 | ||||||||||||||
| Middle East | Israel | Ashkenazi | 100 | NA | 0.00 | 4.0 | ||||||||||||||
| Middle East | Israel | Sephardi | 63 | NA | 0.00 | 1.6 | ||||||||||||||
| Europe | Germany | 88 | NA | 0.00 | 12.5 | |||||||||||||||
| Europe | Norway | 83 | NA | 0.00 | 21.7 | |||||||||||||||
| Europe | Germany | Sorbs | 112 | NA | 0.00 | 63.4 | ||||||||||||||
| Europe | Belarus | 306 | NA | 0.33 | 51.0 | |||||||||||||||
| Europe | Spain | Spanish Basques | 42 | NA | NA | 0.0 | vauthors = Capelli C, Redhead N, Abernethy JK, Gratrix F, Wilson JF, Moen T, Hervig T, Richards M, Stumpf MP, Underhill PA, Bradshaw P, Shaha A, Thomas MG, Bradman N, Goldstein DB | title = A Y chromosome census of the British Isles | journal = Current Biology | volume = 13 | issue = 11 | pages = 979–984 | date = May 2003 | pmid = 12781138 | doi = 10.1016/s0960-9822(03)00373-7 | s2cid = 526263 | doi-access = free | bibcode = 2003CBio...13..979C | hdl = 20.500.11820/8acb01f3-a7c1-45f5-89de-b796266d651e | hdl-access = free }} |
| Europe | British Crown | Channel Islands | 128 | NA | NA | 2.0 | ||||||||||||||
| Europe | England | Chippenham | 52 | NA | NA | 6.0 | ||||||||||||||
| Europe | England | Cornwall | 52 | NA | NA | 6.0 | ||||||||||||||
| Europe | England | Dorchester | 73 | NA | NA | 4.0 | ||||||||||||||
| Europe | England | Faversham | 55 | NA | NA | 2.0 | ||||||||||||||
| Europe | England | Midhurst | 80 | NA | NA | 1.0 | ||||||||||||||
| Europe | England | Morpeth | 95 | NA | NA | 2.0 | ||||||||||||||
| Europe | England | Norfolk | 121 | NA | NA | 2.0 | ||||||||||||||
| Europe | England | Penrith | 90 | NA | NA | 2.0 | ||||||||||||||
| Europe | England | Southwell | 70 | NA | NA | 4.0 | ||||||||||||||
| Europe | England | Uttoxeter | 84 | NA | NA | 0.0 | ||||||||||||||
| Europe | England | York | 46 | NA | NA | 2.0 | ||||||||||||||
| Europe | Denmark/Germany | Denmark/Schleswig-Holstein | 190 | NA | NA | 8.0 | ||||||||||||||
| Europe | Ireland | Castlerea | 43 | NA | NA | 0.0 | ||||||||||||||
| Europe | British Crown | Isle of Man | 62 | NA | NA | 8.0 | ||||||||||||||
| Europe | Norway | 201 | NA | NA | 12.0 | |||||||||||||||
| Europe | Scotland | Orkney | 121 | NA | NA | 7.0 | ||||||||||||||
| Europe | Ireland | Rush, Dublin | 76 | NA | NA | 1.0 | ||||||||||||||
| Europe | Scotland | Durness | 51 | NA | NA | 2.0 | ||||||||||||||
| Europe | Scotland | Oban | 42 | NA | NA | 2.0 | ||||||||||||||
| Europe | Scotland | Pitlochry | 41 | NA | NA | 0.0 | ||||||||||||||
| Europe | Scotland | Stonehaven | 44 | NA | NA | 5.0 | ||||||||||||||
| Europe | Scotland | Western Isles | 88 | NA | NA | 3.0 | ||||||||||||||
| Europe | Scotland | Shetland | 63 | NA | NA | 6.0 | ||||||||||||||
| Europe | Wales | Haverfordwest | 59 | NA | NA | 2.0 | ||||||||||||||
| Europe | Wales | Llangefni | 80 | NA | NA | 1.0 | ||||||||||||||
| Europe | Wales | Llanidloes | 57 | NA | NA | 4.0 | ||||||||||||||
| Europe | Turkey | 523 | NA | NA | 6.9 | vauthors = Cinnioğlu C, King R, Kivisild T, Kalfoğlu E, Atasoy S, Cavalleri GL, Lillie AS, Roseman CC, Lin AA, Prince K, Oefner PJ, Shen P, Semino O, Cavalli-Sforza LL, Underhill PA | title = Excavating Y-chromosome haplotype strata in Anatolia | journal = Human Genetics | volume = 114 | issue = 2 | pages = 127–148 | date = January 2004 | pmid = 14586639 | doi = 10.1007/s00439-003-1031-4 | s2cid = 10763736 }} | |||||
| Europe | Italy | Sicily | 236 | NA | NA | 5.5 | vauthors = Di Gaetano C, Cerutti N, Crobu F, Robino C, Inturri S, Gino S, Guarrera S, Underhill PA, King RJ, Romano V, Cali F, Gasparini M, Matullo G, Salerno A, Torre C, Piazza A | title = Differential Greek and northern African migrations to Sicily are supported by genetic evidence from the Y chromosome | journal = European Journal of Human Genetics | volume = 17 | issue = 1 | pages = 91–99 | date = January 2009 | pmid = 18685561 | pmc = 2985948 | doi = 10.1038/ejhg.2008.120 }} | ||||
| Europe | Greece | 77 | NA | NA | 15.6 | vauthors = Firasat S, Khaliq S, Mohyuddin A, Papaioannou M, Tyler-Smith C, Underhill PA, Ayub Q | title = Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan | journal = European Journal of Human Genetics | volume = 15 | issue = 1 | pages = 121–126 | date = January 2007 | pmid = 17047675 | pmc = 2588664 | doi = 10.1038/sj.ejhg.5201726 }} | |||||
| South Asia | Pakistan | Burusho | 97 | NA | NA | 25.8 | ||||||||||||||
| South Asia | Pakistan | Kalash | 44 | NA | NA | 18.2 | ||||||||||||||
| South Asia | Pakistan | Pathan (Pashtun) | 96 | NA | NA | 44.8 | ||||||||||||||
| South Asia | Pakistan | 638 | NA | NA | 37.1 | |||||||||||||||
| South Asia | Nepal | Tharu from Chitwan District in central Inner Terai ('CI' village sample) | 57 | NA | 0.00 | 10.5 | vauthors = Fornarino S, Pala M, Battaglia V, Maranta R, Achilli A, Modiano G, Torroni A, Semino O, Santachiara-Benerecetti SA | title = Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation | journal = BMC Evolutionary Biology | volume = 9 | issue = 1 | article-number = 154 | date = July 2009 | pmid = 19573232 | pmc = 2720951 | doi = 10.1186/1471-2148-9-154 | bibcode = 2009BMCEE...9..154F | doi-access = free }} | ||
| South Asia | Nepal | Tharu from Chitwan District ('CII' village sample) | 77 | NA | 0.00 | 3.9 | ||||||||||||||
| South Asia | Nepal | Tharu from Morang District in eastern Outer Terai | 37 | NA | 0.00 | 16.2 | ||||||||||||||
| South Asia | Nepal/India | Hindus (as proxy for Indian ancestry) Chitwan District, Nepal | 26 | NA | 0.00 | 69.2 | ||||||||||||||
| South Asia | India | Hindus New Delhi | 49 | NA | 0.00 | 34.7 | ||||||||||||||
| South Asia | India | Andhara Pradesh tribal | 29 | NA | 0.00 | 27.6 | ||||||||||||||
| Europe | Poland | 913 | NA | NA | 57.0 | vauthors = Kayser M, Lao O, Anslinger K, Augustin C, Bargel G, Edelmann J, Elias S, Heinrich M, Henke J, Henke L, Hohoff C, Illing A, Jonkisz A, Kuzniar P, Lebioda A, Lessig R, Lewicki S, Maciejewska A, Monies DM, Pawłowski R, Poetsch M, Schmid D, Schmidt U, Schneider PM, Stradmann-Bellinghausen B, Szibor R, Wegener R, Wozniak M, Zoledziewska M, Roewer L, Dobosz T, Ploski R | title = Significant genetic differentiation between Poland and Germany follows present-day political borders, as revealed by Y-chromosome analysis | journal = Human Genetics | volume = 117 | issue = 5 | pages = 428–443 | date = September 2005 | pmid = 15959808 | doi = 10.1007/s00439-005-1333-9 | s2cid = 11066186 }} | |||||
| Europe | Germany | 1215 | NA | NA | 17.9 | |||||||||||||||
| Europe | Germany | Berlin | 103 | NA | NA | 22.3 | ||||||||||||||
| Europe | Germany | Leipzig | 144 | NA | NA | 27.1 | ||||||||||||||
| Europe | Germany | Magdeburg | 100 | NA | NA | 21 | ||||||||||||||
| Europe | Germany | Rostock | 96 | NA | NA | 31.3 | ||||||||||||||
| Europe | Germany | Greifswald | 104 | NA | NA | 19.2 | ||||||||||||||
| Europe | Germany | Hamburg | 161 | NA | NA | 16.8 | ||||||||||||||
| Europe | Germany | Münster | 102 | NA | NA | 7.8 | ||||||||||||||
| Europe | Germany | Freiburg | 102 | NA | NA | 10.8 | ||||||||||||||
| Europe | Germany | Cologne | 96 | NA | NA | 15.6 | ||||||||||||||
| Europe | Germany | Mainz | 95 | NA | NA | 8.4 | ||||||||||||||
| Europe | Germany | Munich | 95 | NA | NA | 14.3 | ||||||||||||||
| Europe | Greece | Nea Nikomedeia | 57 | NA | 0.00 | 21.1 | vauthors = King RJ, Ozcan SS, Carter T, Kalfoğlu E, Atasoy S, Triantaphyllidis C, Kouvatsi A, Lin AA, Chow CE, Zhivotovsky LA, Michalodimitrakis M, Underhill PA | title = Differential Y-chromosome Anatolian influences on the Greek and Cretan Neolithic | journal = Annals of Human Genetics | volume = 72 | issue = Pt 2 | pages = 205–214 | date = March 2008 | pmid = 18269686 | doi = 10.1111/j.1469-1809.2007.00414.x | s2cid = 22406638 }} | ||||
| Europe | Greece | Sesklo/Dimini | 57 | NA | 0.00 | 10.5 | ||||||||||||||
| Europe | Greece | Lerna/Franchthi | 57 | NA | 0.00 | 1.8 | ||||||||||||||
| Europe | Greece | Crete | 193 | NA | 0.50 | 8.3 | ||||||||||||||
| Europe | Greece | Crete, Heraklion Prefecture | 104 | NA | 0.00 | 8.7 | vauthors = Martinez L, Underhill PA, Zhivotovsky LA, Gayden T, Moschonas NK, Chow CE, Conti S, Mamolini E, Cavalli-Sforza LL, Herrera RJ | title = Paleolithic Y-haplogroup heritage predominates in a Cretan highland plateau | journal = European Journal of Human Genetics | volume = 15 | issue = 4 | pages = 485–493 | date = April 2007 | pmid = 17264870 | doi = 10.1038/sj.ejhg.5201769 | s2cid = 9847088 | doi-access = free }} | |||
| Europe | Greece | Crete, Lasithi Plateau | 41 | NA | 0.00 | 29.3 | ||||||||||||||
| Europe | Greece | Crete, Lasithi Prefecture | 23 | NA | 0.00 | 17.4 | ||||||||||||||
| Europe | Ukraine | 94 | NA | NA | 43.6 | vauthors = Kharkov VN, Stepanov VA, Borinskaya SA, Kozhekbaeva ZM, Gusar VA, Grechanina EY, Puzyrev VP, Khusnutdinova EK, Yankovsky NK | title = Gene pool structure of eastern Ukrainians as inferred from the Y-chromosome haplogroups. | journal = Russian Journal of Genetics | date = March 2004 | volume = 40 | issue = 3 | pages = 326–331 | doi = 10.1023/B:RUGE.0000021635.80528.2f | s2cid = 25907265 }} | ||||||
| Europe | Belarus | 68 | NA | NA | 45.6 | |||||||||||||||
| North Asia | Russia (Altai Republic) | Northern Altaians (Gorno-Altaisk) | 20 | NA | NA | 50.0 | vauthors = Kharkov VN, Stepanov VA, Medvedeva OF, Spiridonova MG, Voevoda MI, Tadinova VN, Puzyrev VP | title = Gene pool differences between northern and southern Altaians inferred from the data on Y-chromosomal haplogroups. | journal = Russian Journal of Genetics | date = May 2007 | volume = 43 | issue = 5 | pages = 551–562 | doi = 10.1134/S1022795407050110 | s2cid = 566825 }} | |||||
| North Asia | Russia (Altai Republic) | Northern Altaians (Kurmach-Baigol) | 11 | NA | NA | 18.2 | ||||||||||||||
| North Asia | Russia (Altai Republic) | Northern Altaians (Turochak) | 19 | NA | NA | 36.8 | ||||||||||||||
| North Asia | Russia (Altai Republic) | Southern Altaians (Beshpel'tir) | 43 | NA | NA | 58.1 | ||||||||||||||
| North Asia | Russia (Altai Republic) | Southern Altaians (Kulada) | 46 | NA | NA | 52.2 | ||||||||||||||
| North Asia | Russia (Altai Republic) | Southern Altaians (Kosh-Agach) | 7 | NA | NA | 28.6 | ||||||||||||||
| Europe | England | West Lancashire (standard 2-G) | 49 | NA | NA | 2.0 | vauthors = Bowden GR, Balaresque P, King TE, Hansen Z, Lee AC, Pergl-Wilson G, Hurley E, Roberts SJ, Waite P, Jesch J, Jones AL, Thomas MG, Harding SE, Jobling MA | title = Excavating past population structures by surname-based sampling: the genetic legacy of the Vikings in northwest England | journal = Molecular Biology and Evolution | volume = 25 | issue = 2 | pages = 301–309 | date = February 2008 | pmid = 18032405 | pmc = 2628767 | doi = 10.1093/molbev/msm255 | ref = | quote = Samples ascertained on the basis of two generations of residence were compared with independent samples based on known ancestry in the region, plus the possession of a surname known from historical records to have been present there in medieval times. }} | ||
| Europe | England | Wirral Peninsula (standard 2-G) | 100 | NA | NA | 4.0 | ||||||||||||||
| Europe | England | West Lancashire (medieval) | 42 | NA | NA | 16.7 | ||||||||||||||
| Europe | England | Wirral Peninsula (medieval) | 37 | NA | NA | 13.5 | ||||||||||||||
| South Asia | India | South India, Chenchu | 41 | NA | NA | 26.8 | vauthors = Kivisild T, Rootsi S, Metspalu M, Mastana S, Kaldma K, Parik J, Metspalu E, Adojaan M, Tolk HV, Stepanov V, Gölge M, Usanga E, Papiha SS, Cinnioğlu C, King R, Cavalli-Sforza L, Underhill PA, Villems R | title = The genetic heritage of the earliest settlers persists both in Indian tribal and caste populations | journal = American Journal of Human Genetics | volume = 72 | issue = 2 | pages = 313–332 | date = February 2003 | pmid = 12536373 | pmc = 379225 | doi = 10.1086/346068 | bibcode = 2003AmJHG..72..313K }} | |||
| South Asia | India | South India, Koya | 41 | NA | NA | 2.4 | ||||||||||||||
| South Asia | India | West Bengal | 31 | NA | NA | 38.7 | ||||||||||||||
| South Asia | India | Konkanastha Brahmins, Bombay | 43 | NA | NA | 41.9 | ||||||||||||||
| South Asia | India | Gujarat | 29 | NA | NA | 24.1 | ||||||||||||||
| South Asia | India | Lambadi | 35 | NA | NA | 8.6 | ||||||||||||||
| South Asia | India | Punjab | 66 | NA | NA | 47.0 | ||||||||||||||
| South Asia | Sri Lanka | Sinhalese | 39 | NA | NA | 12.8 | ||||||||||||||
| North Asia | Russia | Tuvan | 40 | NA | NA | 7.5 | vauthors = Lell JT, Sukernik RI, Starikovskaya YB, Su B, Jin L, Schurr TG, Underhill PA, Wallace DC | title = The dual origin and Siberian affinities of Native American Y chromosomes | journal = American Journal of Human Genetics | volume = 70 | issue = 1 | pages = 192–206 | date = January 2002 | pmid = 11731934 | pmc = 384887 | doi = 10.1086/338457 }} | ||||
| North Asia | Russia | Tofalar | 19 | NA | NA | 5.3 | ||||||||||||||
| North Asia | Russia | Buryat | 13 | NA | NA | 0.0 | ||||||||||||||
| North Asia | Russia | Yenisey Evenk | 31 | NA | NA | 9.7 | ||||||||||||||
| North Asia | Russia | Okhotsk Evenk | 16 | NA | NA | 0.0 | ||||||||||||||
| North Asia | Russia | Ulchi/Nanai | 53 | NA | NA | 0.0 | ||||||||||||||
| North Asia | Russia | Upriver Negidal | 10 | NA | NA | 0.0 | ||||||||||||||
| North Asia | Russia | Downriver Negidal | 7 | NA | NA | 0.0 | ||||||||||||||
| North Asia | Russia | Ugedey | 20 | NA | NA | 5.0 | ||||||||||||||
| North Asia | Russia | Nivkh | 17 | NA | NA | 0.0 | ||||||||||||||
| North Asia | Russia | Kamchatka, Koryak | 27 | NA | NA | 0.0 | ||||||||||||||
| North Asia | Russia | Kamchatka, Itel\'man | 18 | NA | NA | 22.2 | ||||||||||||||
| North Asia | Russia | Chukotka, Chukchi | 24 | NA | NA | 4.2 | ||||||||||||||
| North Asia | Russia | Chukotka, Asiatic Eskimo | 33 | NA | NA | 0.0 | ||||||||||||||
| Caucasus | Russia | Abazinians | 14 | NA | NA | 14.0 | vauthors = Nasidze I, Ling EY, Quinque D, Dupanloup I, Cordaux R, Rychkov S, Naumova O, Zhukova O, Sarraf-Zadegan N, Naderi GA, Asgary S, Sardas S, Farhud DD, Sarkisian T, Asadov C, Kerimov A, Stoneking M | title = Mitochondrial DNA and Y-chromosome variation in the caucasus | journal = Annals of Human Genetics | volume = 68 | issue = Pt 3 | pages = 205–221 | date = May 2004 | pmid = 15180701 | doi = 10.1046/j.1529-8817.2004.00092.x | s2cid = 27204150 | doi-access = free }} | |||
| Caucasus | Russia | Chechenians | 19 | NA | NA | 5.0 | ||||||||||||||
| Caucasus | Russia | Darginians | 26 | NA | NA | 0.0 | ||||||||||||||
| Caucasus | Russia | Ingushians | 22 | NA | NA | 0.0 | ||||||||||||||
| Caucasus | Russia | Kabardinians | 59 | NA | NA | 2.0 | ||||||||||||||
| Caucasus | Russia | Lezgi (Dagestan) | 25 | NA | NA | 0.0 | ||||||||||||||
| Caucasus | Russia | Ossetians (Ardon) | 28 | NA | NA | 4.0 | ||||||||||||||
| Caucasus | Russia | Ossetians (Digora) | 31 | NA | NA | 0.0 | ||||||||||||||
| Caucasus | Russia | Rutulians | 24 | NA | NA | 0.0 | ||||||||||||||
| Caucasus | Georgia | Abkhazians | 12 | NA | NA | 33.0 | ||||||||||||||
| Caucasus | Armenia | Armenians | 100 | NA | NA | 6.0 | ||||||||||||||
| Caucasus | Azerbaijan | Azerbaijanians | 72 | NA | NA | 7.0 | ||||||||||||||
| Caucasus | Georgia | Georgians | 77 | NA | NA | 10.0 | ||||||||||||||
| Europe | Turkey | 39 | NA | NA | 13.0 | |||||||||||||||
| Middle East | Iran | Isfahan | 50 | NA | NA | 18.0 | ||||||||||||||
| Middle East | Iran | Tehran | 80 | NA | NA | 20.0 | ||||||||||||||
| South Asia | Pakistan | Balti | 13 | NA | NA | 15.0 | vauthors = Qamar R, Ayub Q, Mohyuddin A, Helgason A, Mazhar K, Mansoor A, Zerjal T, Tyler-Smith C, Mehdi SQ | title = Y-chromosomal DNA variation in Pakistan | journal = American Journal of Human Genetics | volume = 70 | issue = 5 | pages = 1107–1124 | date = May 2002 | pmid = 11898125 | pmc = 447589 | doi = 10.1086/339929 }} | ||||
| South Asia | Pakistan | Brahui | 110 | NA | NA | 8.2 | ||||||||||||||
| South Asia | Pakistan | Burusho | 94 | NA | NA | 27.7 | ||||||||||||||
| South Asia | Pakistan | Pakistan Hazara | 23 | NA | NA | 60.9 | ||||||||||||||
| South Asia | Pakistan | Kalash | 44 | NA | NA | 9.1 | ||||||||||||||
| South Asia | Pakistan | Pakistan Kashmiri | 12 | NA | NA | 25.0 | ||||||||||||||
| South Asia | Pakistan | Makrani Baluch | 25 | NA | NA | 24.0 | ||||||||||||||
| South Asia | Pakistan | Makrani Negroid | 33 | NA | NA | 18.2 | ||||||||||||||
| South Asia | Pakistan | Pakistan Parsi | 90 | NA | NA | 26.7 | ||||||||||||||
| South Asia | Pakistan | Pathan (Pashtun) | 93 | NA | NA | 10.8 | ||||||||||||||
| South Asia | Pakistan | Pakistan Sindhi | 122 | NA | NA | 12.3 | ||||||||||||||
| Europe | Albania | Albanian | 51 | NA | NA | 9.8 | vauthors = Semino O, Magri C, Benuzzi G, Lin AA, Al-Zahery N, Battaglia V, Maccioni L, Triantaphyllidis C, Shen P, Oefner PJ, Zhivotovsky LA, King R, Torroni A, Cavalli-Sforza LL, Underhill PA, Santachiara-Benerecetti AS | title = Origin, diffusion, and differentiation of Y-chromosome haplogroups E and J: inferences on the neolithization of Europe and later migratory events in the Mediterranean area | journal = American Journal of Human Genetics | volume = 74 | issue = 5 | pages = 1023–1034 | date = May 2004 | pmid = 15069642 | pmc = 1181965 | doi = 10.1086/386295 | bibcode = 2004AmJHG..74.1023S }} | |||
| Europe | France | French Basque | 22 | NA | NA | 0.0 | ||||||||||||||
| Europe | Spain | Spanish Basque | 45 | NA | NA | 0.0 | ||||||||||||||
| Europe | Italy | Calabrian | 37 | NA | NA | 0.0 | ||||||||||||||
| Europe | Spain | Catalan | 24 | NA | NA | 0.0 | ||||||||||||||
| Europe | Italy | Central/Northern | 50 | NA | NA | 4.0 | ||||||||||||||
| Europe | Croatia | Croatian | 58 | NA | NA | 29.3 | ||||||||||||||
| Europe | Czech Republic/Slovakia | Czech/Slovak | 45 | NA | NA | 26.7 | ||||||||||||||
| Europe | Netherlands | Dutch | 27 | NA | NA | 3.7 | ||||||||||||||
| Europe | Georgia | Georgian | 63 | NA | NA | 7.9 | ||||||||||||||
| Europe | Germany | German | 16 | NA | NA | 6.2 | ||||||||||||||
| Europe | Greece | Greek | 76 | NA | NA | 11.8 | ||||||||||||||
| Europe | Hungary | Hungarian | 45 | NA | NA | 60.0 | ||||||||||||||
| Middle East | Lebanon | Lebanese | 31 | NA | NA | 9.7 | ||||||||||||||
| Europe | Republic of Macedonia | Macedonian | 20 | NA | NA | 35.0 | ||||||||||||||
| Europe | Poland | Polish | 55 | NA | NA | 56.4 | ||||||||||||||
| Europe | Saami | 24 | NA | NA | 8.3 | |||||||||||||||
| Europe | Italy | Sardinian | 77 | NA | NA | 0.0 | ||||||||||||||
| Europe | Syria | Syrian | 20 | NA | NA | 10.0 | ||||||||||||||
| Europe | Turkey | Turkish | 30 | NA | NA | 6.6 | ||||||||||||||
| Asia | Russia | Udmurt | 43 | NA | NA | 37.2 | ||||||||||||||
| Europe | Ukraine | Ukrainian | 50 | NA | NA | 54.0 | ||||||||||||||
| South Asia | Pakistan | 85 | NA | NA | 16.5 | vauthors = Sengupta S, Zhivotovsky LA, King R, Mehdi SQ, Edmonds CA, Chow CE, Lin AA, Mitra M, Sil SK, Ramesh A, Usha Rani MV, Thakur CM, Cavalli-Sforza LL, Majumder PP, Underhill PA | title = Polarity and temporality of high-resolution y-chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central Asian pastoralists | journal = American Journal of Human Genetics | volume = 78 | issue = 2 | pages = 202–221 | date = February 2006 | pmid = 16400607 | pmc = 1380230 | doi = 10.1086/499411 | bibcode = 2006AmJHG..78..202S }} | ||||
| South Asia | India | Rajput (of Rajasthan) | 29 | NA | NA | 31.3 | ||||||||||||||
| South Asia | Pakistan | Southern | 91 | NA | NA | 31.9 | ||||||||||||||
| Southeast Asia | Cambodia | 6 | NA | NA | 0.0 | |||||||||||||||
| East Asia | China | 128 | NA | NA | 0.0 | |||||||||||||||
| East Asia | Japan | 23 | NA | NA | 0.0 | |||||||||||||||
| North Asia | Siberia | 18 | NA | NA | 0.0 | |||||||||||||||
| South Asia | India | Tribe (Austro-Asiatic) | 64 | NA | NA | 0.0 | ||||||||||||||
| South Asia | India | Tribe (Dravidian) | 18 | NA | NA | 2.8 | ||||||||||||||
| South Asia | India | Tribe (Tibeto-Burman) | 87 | NA | NA | 4.6 | ||||||||||||||
| South Asia | India | Tribe (Indo-European) | 21 | NA | NA | 19.1 | ||||||||||||||
| South Asia | India | Dravidian Upper Caste | 59 | NA | NA | 28.8 | ||||||||||||||
| South Asia | India | Dravidian Middle Caste | 85 | NA | NA | 11.8 | ||||||||||||||
| South Asia | India | Dravidian Lower Caste | 29 | NA | NA | 24.1 | ||||||||||||||
| South Asia | India | Indo-European Upper Caste | 86 | NA | NA | 45.4 | ||||||||||||||
| South Asia | India | Indo-European Middle Caste | 48 | NA | NA | 50.4 | ||||||||||||||
| South Asia | India | Indo-European Lower Caste | 50 | NA | NA | 26.0 | ||||||||||||||
| South Asia | India | Kashmiri Gujars | 49 | NA | 0.00 | 40.86 | vauthors = Sharma S, Rai E, Sharma P, Jena M, Singh S, Darvishi K, Bhat AK, Bhanwer AJ, Tiwari PK, Bamezai RN | title = The Indian origin of paternal haplogroup R1a1* substantiates the autochthonous origin of Brahmins and the caste system | journal = Journal of Human Genetics | volume = 54 | issue = 1 | pages = 47–55 | date = January 2009 | pmid = 19158816 | doi = 10.1038/jhg.2008.2 | s2cid = 22162114 | doi-access = free }} | |||
| South Asia | India | Kashmiri Pandits | 51 | NA | 3.92 | 19.61 | ||||||||||||||
| South Asia | India | Gujarat Brahmins | 64 | NA | 0.00 | 32.81 | ||||||||||||||
| South Asia | India | Bihar Paswan | 27 | NA | 0.00 | 40.74 | ||||||||||||||
| South Asia | India | Bihar Brahmins | 38 | NA | 0.00 | 60.53 | ||||||||||||||
| South Asia | India | Himachal Pradesh Brahmin | 30 | NA | 0.00 | 47.37 | ||||||||||||||
| South Asia | India | Indian Punjab Brahmins | 49 | NA | 0.00 | 35.71 | ||||||||||||||
| South Asia | India | West Bengal Brahmins | 30 | NA | 0.00 | 72.22 | ||||||||||||||
| South Asia | India | Uttar Pradesh Brahmins | 31 | NA | 0.00 | 67.74 | ||||||||||||||
| South Asia | India | Uttar Pradesh Kols | 38 | NA | 0.00 | 14.81 | ||||||||||||||
| South Asia | India | Madhya Pradesh Saharia | 57 | NA | 22.8 | 28.07 | ||||||||||||||
| South Asia | India | Madhya Pradesh Brahmins | 42 | NA | 0.00 | 38.1 | ||||||||||||||
| South Asia | India | Maharashtra Brahmins | 32 | NA | 0.00 | 43.33 | ||||||||||||||
| Europe | Moldova | Moldavians, Carahasani | 72 | NA | NA | 34.7 | ||||||||||||||
| Europe | Moldava | Moldavians Sofia, Drochia, Moldava | 54 | NA | NA | 20.4 | ||||||||||||||
| Europe | Romania | Dniester-Carpathian region | - | NA | NA | 20.4 | ||||||||||||||
| Europe | Ukraine | Ukrainians, Rașcov (Rashkovo), Camenca district | 53 | NA | NA | 41.5 | ||||||||||||||
| Europe | Moldava | Gagauzes, Kongaz | 48 | NA | NA | 12.5 | ||||||||||||||
| Europe | Ukraine | Gagauzes, Etulia | 41 | NA | NA | 26.8 | ||||||||||||||
| East Asia | China | Dongxiang (Mongolian descent) | 49 | 28.0 | vauthors = Wang W, Wise C, Baric T, Black ML, Bittles AH | title = The origins and genetic structure of three co-resident Chinese Muslim populations: the Salar, Bo'an and Dongxiang | journal = Human Genetics | volume = 113 | issue = 3 | pages = 244–252 | date = August 2003 | pmid = 12759817 | doi = 10.1007/s00439-003-0948-y | s2cid = 11138499 }} | ||||||
| East Asia | China | Salar (Central Asian Turkish descent) | 52 | NA | 17.0 | |||||||||||||||
| East Asia | China | Bo\'an (Bonan) Mongolian descent | 47 | NA | 26.0 | |||||||||||||||
| Caucasus | Armenia | Ararat | 44 | NA | 0.00 | 0.0 | vauthors = Weale ME, Yepiskoposyan L, Jager RF, Hovhannisyan N, Khudoyan A, Burbage-Hall O, Bradman N, Thomas MG | title = Armenian Y chromosome haplotypes reveal strong regional structure within a single ethno-national group | journal = Human Genetics | volume = 109 | issue = 6 | pages = 659–674 | date = December 2001 | pmid = 11810279 | doi = 10.1007/s00439-001-0627-9 | s2cid = 23113666 }} | ||||
| Caucasus | Armenia/Georgia | \"Northern Armenians\" | 189 | NA | 0.53 | 4.2 | ||||||||||||||
| Caucasus | Armenia | Syunik (South Armenia) | 140 | NA | 0.00 | 9.3 | ||||||||||||||
| Caucasus | Azerbaijan/Armenia | Karabakh | 215 | NA | 0.00 | 5.6 | ||||||||||||||
| Middle East | Iran | Isfahan, New Julfa, (Armenian descent) | 56 | NA | 0.00 | 1.8 | ||||||||||||||
| Europe | Turkey | near Armenia | 90 | NA | 1.11 | 3.3 | ||||||||||||||
| Europe | Turkey | Istanbul University | 173 | NA | 0.00 | 10.4 | ||||||||||||||
| Caucasus | Azerbaijan | Baku | 29 | NA | 0.00 | 10.3 | ||||||||||||||
| Middle East | Syria | Damascus University | 44 | NA | 0.00 | 2.3 | ||||||||||||||
| Caucasus | Georgia | Tbilisi | 68 | NA | 0.00 | 4.4 | ||||||||||||||
| Europe | Greece | Athens | 132 | NA | 0.00 | 6.1 | ||||||||||||||
| Europe | Mongolia | soldiers mainly from Khalkh | 402 | NA | 0.00 | 2.5 | ||||||||||||||
| Europe | Hungary | 215 | NA | 1.40 | 24.2 | |||||||||||||||
| Europe | Wales | North Wales | 98 | NA | NA | 1.0 | vauthors = Weale ME, Weiss DA, Jager RF, Bradman N, Thomas MG | title = Y chromosome evidence for Anglo-Saxon mass migration | journal = Molecular Biology and Evolution | volume = 19 | issue = 7 | pages = 1008–1021 | date = July 2002 | pmid = 12082121 | doi = 10.1093/oxfordjournals.molbev.a004160 | doi-access = free }} | ||||
| Europe | England | English Midlands | 136 | NA | NA | 4.4 | ||||||||||||||
| Europe | England | East Anglia | 173 | NA | NA | 4.6 | ||||||||||||||
| Europe | Netherlands | Friesland | 94 | NA | NA | 7.4 | ||||||||||||||
| Europe | Norway | 83 | NA | NA | 21.7 | |||||||||||||||
| Europe | United Kingdom | British | 25 | NA | NA | 0.0 | ||||||||||||||
| Europe | Scotland | Orkney | 26 | NA | NA | 27.0 | ||||||||||||||
| Europe | Russia | Pomor | 28 | NA | NA | 36.0 | ||||||||||||||
| Europe | Russia | Russian, North | 49 | NA | NA | 43.0 | ||||||||||||||
| Asia | Russia | Russian, Tashkent | 89 | NA | NA | 47.0 | ||||||||||||||
| Europe | Russia | Kazan Tatar | 38 | NA | NA | 24.0 | ||||||||||||||
| Europe | Russia | Saami | 23 | NA | NA | 22.0 | ||||||||||||||
| Asia | Russia | Nenets | 54 | NA | NA | 11.0 | ||||||||||||||
| Middle East | Lebanon | 50 | NA | NA | 0.0 | |||||||||||||||
| Middle East | Iran | Tehran | 24 | NA | NA | 4.0 | ||||||||||||||
| Middle East | Iran | Shiraz | 12 | NA | NA | 0.0 | ||||||||||||||
| Middle East | Iran | Esfahan | 16 | NA | NA | 0.0 | ||||||||||||||
| Caucasus | Georgia | Svans (Svanetians) | 25 | NA | NA | 8.0 | ||||||||||||||
| Caucasus | Georgia | Kazbegi | 25 | NA | NA | 4.0 | ||||||||||||||
| Caucasus | Georgia | South Ossetians | 17 | NA | NA | 6.0 | ||||||||||||||
| Caucasus | Azerbaijan | Lezgi in Azerbaijan | 12 | NA | NA | 8.0 | ||||||||||||||
| Caucasus | Azerbaijan | Azerbaijanians | 21 | NA | NA | 10.0 | ||||||||||||||
| Caucasus | Armenia | Armenians | 47 | NA | NA | 9.0 | ||||||||||||||
| Central Asia | Afghanistan | Pashtuns | 49 | NA | NA | 51.02 | vauthors = Haber M, Platt DE, Ashrafian Bonab M, Youhanna SC, Soria-Hernanz DF, Martínez-Cruz B, Douaihy B, Ghassibe-Sabbagh M, Rafatpanah H, Ghanbari M, Whale J, Balanovsky O, Wells RS, Comas D, Tyler-Smith C, Zalloua PA | title = Afghanistan's ethnic groups share a Y-chromosomal heritage structured by historical events | journal = PLOS ONE | volume = 7 | issue = 3 | article-number=e34288 | date = 2012 | pmid = 22470552 | pmc = 3314501 | doi = 10.1371/journal.pone.0034288 | bibcode = 2012PLoSO...734288H | doi-access = free }} | ||
| Central Asia | Afghanistan | Tajiks | 56 | NA | NA | 30.36 | ||||||||||||||
| Central Asia | Afghanistan | Hazara | 60 | NA | NA | 6.66 | ||||||||||||||
| Central Asia | Afghanistan | Uzbeks | 17 | NA | NA | 17.64 | ||||||||||||||
| Central Asia | Afghanistan | Balochs | 13 | NA | NA | 0.0 | ||||||||||||||
| Central Asia | Afghanistan | Nuristanis | 5 | NA | NA | 60.0 | ||||||||||||||
| Central Asia | Turkmenistan | Turkmen | 30 | NA | NA | 7.0 | ||||||||||||||
| Central Asia | Turkmenistan | Turkmenistan Kurd | 17 | NA | NA | 12.0 | ||||||||||||||
| Central Asia | Uzbekistan | Sinte Romani | 15 | NA | NA | 0.0 | ||||||||||||||
| Central Asia | Uzbekistan | Iranian (Samarkand) | 53 | NA | NA | 11.0 | ||||||||||||||
| Central Asia | Uzbekistan | Tajik (Samarkand) | 40 | NA | NA | 25.0 | ||||||||||||||
| Central Asia | Uzbekistan | Arab Bukhara | 42 | NA | NA | 19.0 | ||||||||||||||
| Central Asia | Uzbekistan | Crimean Tartar | 22 | NA | NA | 32.0 | ||||||||||||||
| Central Asia | Uzbekistan | Karakalpak | 44 | NA | NA | 18.0 | ||||||||||||||
| Central Asia | Uzbekistan | Uzbek/ Kashkadarya | 19 | NA | NA | 16.0 | ||||||||||||||
| Central Asia | Uzbekistan | Uzbek/ Bukhara | 58 | NA | NA | 28.0 | ||||||||||||||
| Central Asia | Uzbekistan | Uzbek/ Surkhandarya | 68 | NA | NA | 29.0 | ||||||||||||||
| Central Asia | Uzbekistan | Uzbek/ Khorezm | 70 | NA | NA | 30.0 | ||||||||||||||
| Central Asia | Uzbekistan | Uzbek/ Tashkent | 43 | NA | NA | 28.0 | ||||||||||||||
| Central Asia | Uzbekistan | Uzbek/ Fergana Valley | 63 | NA | NA | 22.0 | ||||||||||||||
| Central Asia | Uzbekistan | Samarkand | 45 | NA | NA | 13.0 | ||||||||||||||
| Central Asia | Tajikistan | (near Afghanistan) | 25 | NA | NA | 68.0 | ||||||||||||||
| Central Asia | Tajikistan | Bartangi | 30 | NA | NA | 40.0 | ||||||||||||||
| Central Asia | Tajikistan | Shugnan | 44 | NA | NA | 23.0 | ||||||||||||||
| Central Asia | Tajikistan | Yagnobi | 31 | NA | NA | 16.0 | ||||||||||||||
| Central Asia | Tajikistan | Tajiks/Panjikent | 22 | NA | NA | 64.0 | ||||||||||||||
| Central Asia | Tajikistan | Tajiks/Dushanbe | 16 | NA | NA | 19.0 | ||||||||||||||
| Central Asia | Kyrgyzstan | Kyrgyz | 52 | NA | NA | 63.0 | ||||||||||||||
| Central Asia | Kyrgyzstan | Dungan (Sino-Tibetan) | 40 | NA | NA | 10.0 | ||||||||||||||
| Central Asia | Kazakhstan | Kazakhs | 54 | NA | NA | 4.0 | ||||||||||||||
| Central Asia | Kazakhstan | Uighur | 41 | NA | NA | 22.0 | ||||||||||||||
| South Asia | India | South India Sourashtran | 46 | NA | NA | 39.0 | ||||||||||||||
| South Asia | India | South India Kallar Dravidian | 84 | NA | NA | 4.0 | ||||||||||||||
| South Asia | India | South India Yadhava | 129 | NA | NA | 13.0 | ||||||||||||||
| North Asia | Russia | Tuvinian | 42 | NA | NA | 14.0 | ||||||||||||||
| North Asia | Mongolia | 24 | NA | NA | 4.0 | |||||||||||||||
| East Asia | Korea | 45 | NA | NA | 0.0 | |||||||||||||||
| East Asia | China | Liqian from Yongchang | 87 | NA | NA | 1.1 | vauthors = Zhou R, An L, Wang X, Shao W, Lin G, Yu W, Yi L, Xu S, Xu J, Xie X | title = Testing the hypothesis of an ancient Roman soldier origin of the Liqian people in northwest China: a Y-chromosome perspective | journal = Journal of Human Genetics | volume = 52 | issue = 7 | pages = 584–591 | date = 2007 | pmid = 17579807 | doi = 10.1007/s10038-007-0155-0 | s2cid = 37658783 | doi-access = free }} | |||
| East Asia | China | Yugur from Sunan in Gansu | 52 | NA | NA | 1.9 | ||||||||||||||
| East Asia | China | Tibetan from Guide, Qinghai | 39 | NA | NA | 2.6 | ||||||||||||||
| East Asia | China | Uyghurs from Urumqi | 49 | NA | NA | NA | ||||||||||||||
| Europe | Italy | Sardinia | 10 | 0.0 | NA | NA | vauthors = Rosser ZH, Zerjal T, Hurles ME, Adojaan M, Alavantic D, Amorim A, Amos W, Armenteros M, Arroyo E, Barbujani G, Beckman G, Beckman L, Bertranpetit J, Bosch E, Bradley DG, Brede G, Cooper G, Côrte-Real HB, de Knijff P, Decorte R, Dubrova YE, Evgrafov O, Gilissen A, Glisic S, Gölge M, Hill EW, Jeziorowska A, Kalaydjieva L, Kayser M, Kivisild T, Kravchenko SA, Krumina A, Kucinskas V, Lavinha J, Livshits LA, Malaspina P, Maria S, McElreavey K, Meitinger TA, Mikelsaar AV, Mitchell RJ, Nafa K, Nicholson J, Nørby S, Pandya A, Parik J, Patsalis PC, Pereira L, Peterlin B, Pielberg G, Prata MJ, Previderé C, Roewer L, Rootsi S, Rubinsztein DC, Saillard J, Santos FR, Stefanescu G, Sykes BC, Tolun A, Villems R, Tyler-Smith C, Jobling MA | title = Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language | journal = American Journal of Human Genetics | volume = 67 | issue = 6 | pages = 1526–1543 | date = December 2000 | pmid = 11078479 | pmc = 1287948 | doi = 10.1086/316890 }} | ||||
| Europe | England | Cornwall | 51 | 0.0 | NA | NA | ||||||||||||||
| Europe | Spain | Basque | 26 | 0.0 | NA | NA | ||||||||||||||
| Europe | Portugal | Northern | 328 | 0.0 | NA | NA | ||||||||||||||
| North Africa | Algeria | 27 | 0.0 | NA | NA | |||||||||||||||
| North Africa | 129 | 0.0 | NA | NA | ||||||||||||||||
| North Africa | Tunisia | 'Jerbian' Arabs (from the island of Djerba) | 46 | NA | 4.3 | 4.3 | ||||||||||||||
| Europe | Finland | 57 | 10.0 | NA | NA | |||||||||||||||
| Europe | Bulgaria | 24 | 12.0 | NA | NA | |||||||||||||||
| Europe | Netherlands | 84 | 13.0 | NA | NA | |||||||||||||||
| Europe | Germany | Bavarian | 80 | 15.0 | NA | NA | ||||||||||||||
| Europe | Sweden | Gotlander | 64 | 16.0 | NA | NA | ||||||||||||||
| Europe | Yugoslavian | 100 | 16.0 | NA | NA | |||||||||||||||
| Europe | Russia | Chuvash | 17 | 18.0 | NA | NA | ||||||||||||||
| Europe | Sweden | Northern | 48 | 19.0 | NA | NA | ||||||||||||||
| Europe | Romania | 45 | 20.0 | NA | NA | |||||||||||||||
| Europe | Iceland | 28 | 21.0 | NA | NA | |||||||||||||||
| Europe | Saami | 48 | 21.0 | NA | NA | |||||||||||||||
| Europe | Hungary | 36 | 22.0 | NA | NA | |||||||||||||||
| Europe | Estonia | 207 | 27.0 | NA | NA | |||||||||||||||
| Europe | Russia | Mari | 48 | 29.0 (Tambets disagrees) | NA | NA | ||||||||||||||
| Europe | Ukraine | Ukraine | 27 | 30.0 | NA | NA | ||||||||||||||
| Europe | Germany | 30 | 30.0 | NA | NA | |||||||||||||||
| Europe | Norway | 52 | 31.0 | NA | NA | |||||||||||||||
| Europe | Lithuania | 38 | 34.0 | NA | NA | |||||||||||||||
| Europe | Slovenia | 70 | 37.0 | NA | NA | |||||||||||||||
| Europe | Czech Republic | 53 | 38.0 | NA | NA | |||||||||||||||
| Europe | Belarus | 41 | 39.0 | NA | NA | |||||||||||||||
| Europe | Latvia | 34 | 41.0 | NA | NA | |||||||||||||||
| Asia | Russia | 122 | 47.0 | NA | NA | |||||||||||||||
| Europe | Slovakia | 70 | 47.0 | NA | NA | |||||||||||||||
| Europe | Poland | 112 | 54.0 | NA | NA | |||||||||||||||
| Europe | Ireland | 57 | 1.0 | NA | NA | |||||||||||||||
| Europe | Ossetia | 47 | 2.0 | NA | NA | |||||||||||||||
| Europe | Cyprus | 45 | 2.0 | NA | NA | |||||||||||||||
| Europe | Italy | 99 | 2.0 | NA | NA | |||||||||||||||
| Europe | Spain | 126 | 2.0 | NA | NA | |||||||||||||||
| Europe | Portugal | Southern | 57 | 2.0 | NA | NA | ||||||||||||||
| Europe | Belgium | 92 | 4.0 | NA | NA | |||||||||||||||
| Europe | Turkey | 167 | 5.0 | NA | NA | |||||||||||||||
| Europe | France | 40 | 5.0 | NA | NA | |||||||||||||||
| Europe | Georgia | 64 | 6.0 | NA | NA | |||||||||||||||
| Europe | Armenia | 89 | 6.0 | NA | NA | |||||||||||||||
| Europe | Denmark | 56 | 7.0 | NA | NA | |||||||||||||||
| Europe | Scotland | Western | 120 | 7.0 | NA | NA | ||||||||||||||
| Europe | Scotland | 43 | 7.0 | NA | NA | |||||||||||||||
| Europe | Greece | 36 | 8.0 | NA | NA | |||||||||||||||
| Europe | England | East Anglia | 172 | 9.0 | NA | NA | ||||||||||||||
| Europe | Iceland | 181 | 23.8 | NA | NA | vauthors = Helgason A, Sigureth ardóttir S, Nicholson J, Sykes B, Hill EW, Bradley DG, Bosnes V, Gulcher JR, Ward R, Stefánsson K | title = Estimating Scandinavian and Gaelic ancestry in the male settlers of Iceland | journal = American Journal of Human Genetics | volume = 67 | issue = 3 | pages = 697–717 | date = September 2000 | pmid = 10931763 | pmc = 1287529 | doi = 10.1086/303046 }} | |||||
| Europe | Norway | 112 | 17.9 | NA | NA | |||||||||||||||
| Europe | Sweden | 110 | 17.3 | NA | NA | |||||||||||||||
| Europe | Denmark | 12 | 16.7 | NA | NA | |||||||||||||||
| Europe | Ireland | 222 | 0.5 | NA | NA | |||||||||||||||
| Europe | Scotland | 61 | 6.6 | NA | NA | |||||||||||||||
| Europe | Britain | 32 | 9.4 | NA | NA | |||||||||||||||
| Europe | Germany | 32 | 9.4 | NA | NA | |||||||||||||||
| Europe | Greece | 42 | 4.8 | NA | NA | |||||||||||||||
| Europe | Italy | 332 | 2.7 | NA | NA | |||||||||||||||
| Asia | Russia | 30 | 43.3 | NA | NA | |||||||||||||||
| Europe | Estonia | 74 | 36.5 | NA | NA | |||||||||||||||
| Europe | Russia | Komi-Permyaks | 42 | 23.8 | NA | NA | ||||||||||||||
| Europe | Russia | Russian (Perm) | 37 | 43.2 | NA | NA | ||||||||||||||
| Europe | Russia - Mordovia | Mordovian Erzya | 46 | 39.1 | NA | NA | ||||||||||||||
| Europe | Russia - Mordovia | Mordovian Moksi | 46 | 21.7 | NA | NA | ||||||||||||||
| Europe | Estonia | Estonia Russian | 26 | 26.9 | NA | NA | ||||||||||||||
| Europe | Ukraine | Ukrainian | 6 | 50.0 | NA | NA | ||||||||||||||
| Europe | Bulgaria | Bulgarian | 808 | 17.5 | NA | NA | vauthors = Karachanak S, Grugni V, Fornarino S, Nesheva D, Al-Zahery N, Battaglia V, Carossa V, Yordanov Y, Torroni A, Galabov AS, Toncheva D, Semino O | title = Y-chromosome diversity in modern Bulgarians: new clues about their ancestry | journal = PLOS ONE | volume = 8 | issue = 3 | article-number=e56779 | date = 2013 | pmid = 23483890 | pmc = 3590186 | doi = 10.1371/journal.pone.0056779 | bibcode = 2013PLoSO...856779K | doi-access = free }} | ||
| Europe | Turkey | Northeast Turkish | 11 | 18.2 | NA | NA | ||||||||||||||
| Europe | Turkey | Central Anatolian | 18 | 11.1 | NA | NA | ||||||||||||||
| Europe | Turkey | Southwest Turkish | 29 | 10.3 | NA | NA | ||||||||||||||
| Europe | Turkey | Southeast Turkish | 13 | 15.4 | NA | NA | ||||||||||||||
| Europe | Cyprus | Turkish Cypriots | 22 | 13.6 | NA | NA | ||||||||||||||
| Middle East | Talysh | 20 | 10.0 | NA | NA | vauthors = Di Giacomo F, Luca F, Popa LO, Akar N, Anagnou N, Banyko J, Brdicka R, Barbujani G, Papola F, Ciavarella G, Cucci F, Di Stasi L, Gavrila L, Kerimova MG, Kovatchev D, Kozlov AI, Loutradis A, Mandarino V, Mammi' C, Michalodimitrakis EN, Paoli G, Pappa KI, Pedicini G, Terrenato L, Tofanelli S, Malaspina P, Novelletto A | title = Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe | journal = Human Genetics | volume = 115 | issue = 5 | pages = 357–371 | date = October 2004 | pmid = 15322918 | doi = 10.1007/s00439-004-1168-9 | s2cid = 18482536 }} | |||||
| Caucasus | Azerbaijan | Azeri | 24 | 12.5 | NA | NA | ||||||||||||||
| Europe | Croatia | Mainland | 108 | 34.3 | NA | NA | vauthors = Pericić M, Lauc LB, Klarić IM, Rootsi S, Janićijevic B, Rudan I, Terzić R, Colak I, Kvesić A, Popović D, Sijacki A, Behluli I, Dordevic D, Efremovska L, Bajec DD, Stefanović BD, Villems R, Rudan P | title = High-resolution phylogenetic analysis of southeastern Europe traces major episodes of paternal gene flow among Slavic populations | journal = Molecular Biology and Evolution | volume = 22 | issue = 10 | pages = 1964–1975 | date = October 2005 | pmid = 15944443 | doi = 10.1093/molbev/msi185 | doi-access = free }} | ||||
| Europe | Bosnia-Herzogivina | Bosnians | 69 | 24.6 | NA | NA | ||||||||||||||
| Europe | Bosnia-Herzogivina | Herzogivinians | 141 | 12.1 | NA | NA | ||||||||||||||
| Europe | Serbia | Serbians | 113 | 15.9 | NA | NA | ||||||||||||||
| Europe | Kosova | Albanians | 114 | 4.4 | NA | NA | ||||||||||||||
| Europe | Republic of Macedonia | Macedonians | 79 | 15.2 | NA | NA | ||||||||||||||
| Europe | Republic of Macedonia | Romani | 57 | 1.8 | NA | NA | ||||||||||||||
| Europe | Croatia | Mainland | 109 | 33.9 | NA | NA | ||||||||||||||
| Europe | Croatia | Krk | 74 | 28.0 | NA | NA | ||||||||||||||
| Europe | Croatia | Brač | 49 | 13.0 | NA | NA | ||||||||||||||
| Europe | Croatia | Hvar | 91 | 8.0 | NA | NA | ||||||||||||||
| Europe | Croatia | Korčula | 134 | 27.0 | NA | NA | ||||||||||||||
| Europe | Russia | North | 380 | 34.20 | NA | NA | vauthors = Balanovsky O, Rootsi S, Pshenichnov A, Kivisild T, Churnosov M, Evseeva I, Pocheshkhova E, Boldyreva M, Yankovsky N, Balanovska E, Villems R | title = Two sources of the Russian patrilineal heritage in their Eurasian context | journal = American Journal of Human Genetics | volume = 82 | issue = 1 | pages = 236–250 | date = January 2008 | pmid = 18179905 | pmc = 2253976 | doi = 10.1016/j.ajhg.2007.09.019 }} | ||||
| Europe | Russia | Central | 364 | 46.50 | NA | NA | ||||||||||||||
| Europe | Russia | South | 484 | 55.40 | NA | NA | ||||||||||||||
| Europe | Portugal | 553 | 1.27 | NA | NA | |||||||||||||||
| Europe | Sweden | Swedes | 141 | 18.4 | NA | NA | vauthors = Tambets K, Rootsi S, Kivisild T, Help H, Serk P, Loogväli EL, Tolk HV, Reidla M, Metspalu E, Pliss L, Balanovsky O, Pshenichnov A, Balanovska E, Gubina M, Zhadanov S, Osipova L, Damba L, Voevoda M, Kutuev I, Bermisheva M, Khusnutdinova E, Gusar V, Grechanina E, Parik J, Pennarun E, Richard C, Chaventre A, Moisan JP, Barác L, Pericić M, Rudan P, Terzić R, Mikerezi I, Krumina A, Baumanis V, Koziel S, Rickards O, De Stefano GF, Anagnou N, Pappa KI, Michalodimitrakis E, Ferák V, Füredi S, Komel R, Beckman L, Villems R | title = The western and eastern roots of the Saami--the story of genetic "outliers" told by mitochondrial DNA and Y chromosomes | journal = American Journal of Human Genetics | volume = 74 | issue = 4 | pages = 661–682 | date = April 2004 | pmid = 15024688 | doi = 10.1086/383203 | pmc = 1181943 | ref = }} | |||
| Europe | Estonia | Estonians | 209 | 33.5 | NA | NA | ||||||||||||||
| Europe | Latvia | Latvians | 86 | 38.4 | NA | NA | ||||||||||||||
| Europe | Russia | Mari | 111 | 47.7 (Rosser disagrees) | NA | NA | ||||||||||||||
| Europe | Russia | Mordvin | 83 | 26.5 | NA | NA | ||||||||||||||
| Europe | Russia | Komi | 94 | 33 | NA | NA | ||||||||||||||
| Europe | Russia | Udmurt | 87 | 10.3 | NA | NA | ||||||||||||||
| Europe | Russia | Chuvash | 79 | 31.6 | NA | NA | ||||||||||||||
| Europe | Russia | Volga Tatars | 126 | 34.1 | NA | NA | ||||||||||||||
| Europe | France | French | 61 | 0 | NA | NA | ||||||||||||||
| Europe | Hungary | Hungarians | 113 | 20.4 | NA | NA | ||||||||||||||
| Europe | Russia | Russians | 61 | 42.6 | NA | NA | ||||||||||||||
| North Asia | Russia | Khant | 47 | 4.3 | NA | NA | ||||||||||||||
| North Asia | Russia | Nganasan | 38 | 0 | NA | NA | ||||||||||||||
| North Asia | Russia | Nenets | 148 | 0 | NA | NA | ||||||||||||||
| North Asia | Russia | Selkup | 131 | 19.1 | NA | NA | ||||||||||||||
| North Asia | Russia | Ket | 48 | 0 | NA | NA | ||||||||||||||
| North Asia | Russia | Dolgan | 67 | 16.4 | NA | NA | ||||||||||||||
| North Asia | Russia | Yakut | 155 | 1.9 | NA | NA | ||||||||||||||
| North Asia | Russia | Buryat | 81 | 1.2 | NA | NA | ||||||||||||||
| North Asia | Russia | Evenk | 96 | 1 | NA | NA | ||||||||||||||
| North Asia | Russia | Evens | 31 | 6.5 | NA | NA | ||||||||||||||
| North Asia | Russia | Altaians | 98 | 46.9 | NA | NA | ||||||||||||||
| Europe | Norway | Norwegians | 72 | 23.6 | NA | NA | ||||||||||||||
| Europe | Denmark | Danes | 194 | 16.5 | NA | NA | ||||||||||||||
| Europe | Turkey | Kurds Zazaki speakers | 27 | NA | NA | 25.9 | vauthors = Nasidze I, Quinque D, Ozturk M, Bendukidze N, Stoneking M | title = MtDNA and Y-chromosome variation in Kurdish groups | journal = Annals of Human Genetics | volume = 69 | issue = Pt 4 | pages = 401–412 | date = July 2005 | pmid = 15996169 | doi = 10.1046/j.1529-8817.2005.00174.x | s2cid = 23771698 }} | ||||
| Europe | Turkey | Kurds Kurmanji speakers | 87 | NA | NA | 12.7 | ||||||||||||||
| Middle East | Iraq | Kurds | 95 | NA | NA | 11.6 | vauthors = Brinkmann C, Forster P, Schürenkamp M, Horst J, Rolf B, Brinkmann B | title = Human Y-chromosomal STR haplotypes in a Kurdish population sample | journal = International Journal of Legal Medicine | volume = 112 | issue = 3 | pages = 181–183 | date = 1999 | pmid = 10335882 | doi = 10.1007/s004140050228 | s2cid = 25668279 }} | ||||
| Caucasus | Georgia | Kurds | 25 | NA | NA | 0.0 | ||||||||||||||
| Middle East | Jordan | Amman | 101 | NA | NA | 2.0 | ||||||||||||||
| Middle East | Jordan | Dead Sea | 45 | NA | NA | 0.0 | ||||||||||||||
| Middle East | Iraq | Baghdad, different ethnic groups | 139 | NA | NA | 6.5 | ||||||||||||||
| Europe | Russia | Arkhangelsk | 28 | NA | 0.00 | 17.9 | vauthors = Mirabal S, Regueiro M, Cadenas AM, Cavalli-Sforza LL, Underhill PA, Verbenko DA, Limborska SA, Herrera RJ | title = Y-chromosome distribution within the geo-linguistic landscape of northwestern Russia | journal = European Journal of Human Genetics | volume = 17 | issue = 10 | pages = 1260–1273 | date = October 2009 | pmid = 19259129 | pmc = 2986641 | doi = 10.1038/ejhg.2009.6 }} | ||||
| North Asia | Russia | Khanty | 27 | NA | 0.00 | 14.8 | ||||||||||||||
| Europe | Russia (Komi Republic) | Izhma Komi from Izhemsky District | 54 | NA | 0.00 | 29.6 | ||||||||||||||
| Europe | Russia (Komi Republic) | Komi from Priluzsky District | 49 | NA | 0.00 | 32.7 | ||||||||||||||
| Europe | Russia | Kursk region Russian | 40 | NA | 0.00 | 52.5 | ||||||||||||||
| Europe | Russia | Tver region Russian | 38 | NA | 0.00 | 57.9 |
| Continent | Population | #No. | Total% | R-P25* | R-V88 | R-M269 | R-M73 |
|---|---|---|---|---|---|---|---|
| Africa | Northern Africa | 691 | 5.9% | 0.0% | 5.2% | 0.7% | 0.0% |
| Africa | Central Sahel Region | 461 | 23.0% | 0.0% | 23.0% | 0.0% | 0.0% |
| Africa | Western Africa | 123 | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
| Africa | Eastern Africa | 442 | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
| Africa | Southern Africa | 105 | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
| Europe | Western Europeans | 465 | 57.8% | 0.0% | 0.0% | 57.8% | 0.0% |
| Europe | North western Europeans | 43 | 55.8% | 0.0% | 0.0% | 55.8% | 0.0% |
| Europe | Central Europeans | 77 | 42.9% | 0.0% | 0.0% | 42.9% | 0.0% |
| Europe | North Eastern Europeans | 74 | 1.4% | 0.0% | 0.0% | 1.4% | 0.0% |
| Europe | Russians | 60 | 6.7% | 0.0% | 0.0% | 6.7% | 0.0% |
| Europe | Eastern Europeans | 149 | 20.8% | 0.0% | 0.0% | 20.8% | 0.0% |
| Europe | South eastern Europeans | 510 | 13.1% | 0.0% | 0.2% | 12.9% | 0.0% |
| Asia | Western Asians | 328 | 5.8% | 0.0% | 0.3% | 5.5% | 0.0% |
| Asia | Southern Asians | 288 | 4.8% | 0.0% | 0.0% | 1.7% | 3.1% |
| Asia | South eastern Asians | 10 | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
| Asia | North eastern Asians | 30 | 0.0% | 0.0% | 0.0% | 0.0% | 0.0% |
| Asia | Eastern Asians | 156 | 0.6% | 0.0% | 0.0% | 0.6% | 0.0% |
| TOTAL | 5326 |
R2
Haplogroup R2 is most common in South Asia and south Central Asia, as well as diaspora populations, such as the Romanis.
| Tibeto-Burman | Austro-Asiatic | Dravidian | Indo-European | Tribe | Lower Caste | Middle Caste | Upper Caste |
|---|---|---|---|---|---|---|---|
| 5.75% | 10.94% | 5.00% | - | ||||
| - | - | 13.79% | 10.00% | ||||
| - | - | 3.53% | 18.75% | ||||
| - | - | 10.17% | 16.28% |
| Count | Sample Size | R-M124 Frequency % | UAE | vauthors = Cadenas AM, Zhivotovsky LA, Cavalli-Sforza LL, Underhill PA, Herrera RJ | title = Y-chromosome diversity characterizes the Gulf of Oman. | journal = European Journal of Human Genetics | date = March 2008 | volume = 16 | issue = 3 | pages = 374–386 | doi = 10.1038/sj.ejhg.5201934 | pmid = 17928816 | s2cid = 32386262 | doi-access = free }} | vauthors = Mohammad T, Xue Y, Evison M, Tyler-Smith C | title = Genetic structure of nomadic Bedouin from Kuwait | journal = Heredity | volume = 103 | issue = 5 | pages = 425–433 | date = November 2009 | pmid = 19639002 | pmc = 2869035 | doi = 10.1038/hdy.2009.72 | bibcode = 2009Hered.103..425M }} | Yemen | vauthors = Flores C, Maca-Meyer N, Larruga JM, Cabrera VM, Karadsheh N, Gonzalez AM | title = Isolates in a corridor of migrations: a high-resolution analysis of Y-chromosome variation in Jordan | journal = Journal of Human Genetics | volume = 50 | issue = 9 | pages = 435–441 | date = 2005 | pmid = 16142507 | doi = 10.1007/s10038-005-0274-4 | s2cid = 6490283 | doi-access = free }} | Lebanon | vauthors = Myres NM, Rootsi S, Lin AA, Järve M, King RJ, Kutuev I, Cabrera VM, Khusnutdinova EK, Pshenichnov A, Yunusbayev B, Balanovsky O, Balanovska E, Rudan P, Baldovic M, Herrera RJ, Chiaroni J, Di Cristofaro J, Villems R, Kivisild T, Underhill PA | title = A major Y-chromosome haplogroup R1b Holocene era founder effect in Central and Western Europe | journal = European Journal of Human Genetics | volume = 19 | issue = 1 | pages = 95–101 | date = January 2011 | pmid = 20736979 | pmc = 3039512 | doi = 10.1038/ejhg.2010.146 }} | vauthors = Luis JR, Rowold DJ, Regueiro M, Caeiro B, Cinnioğlu C, Roseman C, Underhill PA, Cavalli-Sforza LL, Herrera RJ | title = The Levant versus the Horn of Africa: evidence for bidirectional corridors of human migrations | journal = American Journal of Human Genetics | volume = 74 | issue = 3 | pages = 532–544 | date = March 2004 | pmid = 14973781 | pmc = 1182266 | doi = 10.1086/382286 }} |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8 | 217 | 3.69% | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 1 | 72 | 1.39% | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 1 | 153 | 0.65% | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 1 | 104 | 0.96% | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 2 | 146 | 1.37% | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 2 | 935 | 0.21% | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 1 | 49 | 2.04% | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 1 | 147 | 0.68% |
| R2b% | Population |
|---|---|
| 10.3% | Burusho |
| 6.8% | Kalash |
| 1.0% | Pashtuns |
| 3.4% | Gujarat |
| 0.63% | Pakistan |
P2a~ (P-B253)
The Aeta (or Agta) people of Luzon in the Philippines have also provided the only known samples of P2a~ (P-B253).
Notes
References
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