Haplogroup O-M176

Haplogroup O-M176 (aka O-SRY465) or O1b2 is a human Y-chromosome DNA haplogroup. It is best known for its part in the settlement of Korea and Japan. It is a descendant of Haplogroup O-P31, and it has been estimated to share a most recent common ancestor with its nearest outgroup, Haplogroup O-K18, approximately 28,300 [95% CI 26,100 <-> 30,500] years before present,[3] approximately 29,100 years before present,[2] or approximately 31,108 (95% CI 22,844 <-> 34,893) years before present.[1]

Haplogroup O-M176
O1b2-M176
Possible time of origin31,108 (95% CI 22,844 <-> 34,893) years ago[1]

29,100 years ago[2]

28,300 [95% CI 26,100 <-> 30,500] years ago[3]
Coalescence age25,800 [95% CI 23,400 <-> 28,400] years[3]

25,660 years[2]
Possible place of originManchuria or a nearby part of northern East Asia[4][5]
AncestorO-P31
Defining mutationsM176/SRY465, P49, 022454
Highest frequenciesJapanese, Koreans, Ryukyuans, Manchus

Distribution

Haplogroup O-M176 is found mainly in the northernmost parts of East Asia, from the Uriankhai and Zakhchin peoples of western Mongolia (Katoh et al. 2005) to the Japanese of Japan, though it also has been detected sporadically in the Buryats (Jin et al. 2003). It's been detected with moderate frequencies in Udegeys (Jin, Kim & Kim 2010) of southern Siberia, rarely among populations of Southeast Asia including Indonesia (Hammer et al. 2006 and Jin et al. 2003), the Philippines (Jin et al. 2003), Thailand (Jin et al. 2003), and Vietnam (Hammer et al. 2006 and Jin et al. 2003), and Micronesians (Hammer et al. 2006). This haplogroup is found with its highest frequency and diversity values among modern populations of Japan and Korea and is rare in most populations in China. Among Han Chinese, it has been detected in some samples of Han Chinese from Beijing (1/51, Jin et al. 2003 and Kim et al. 2011),[4] Xi'an (1/34, Kim et al. 2011),[4] one Han Chinese in Henan,[15] Han Chinese in Taiwan (2/352 = 0.57%, including one of 34 Hakka people and one of 258 miscellaneous Han volunteers),[16] Han Chinese from East China sampled from the infertility clinic at the Affiliated Hospitals of Nanjing Medical University at Jiangsu (6/1147 = 0.52%, Lu et al. 2009), Wuhan (1/160),[17] and South China outside of Jiangsu, Anhui, Zhejiang, and Shanghai (1/65).[18] Among ethnic minorities in China, haplogroup O-M176 has been detected with high frequency in samples of Koreans in China (Xue et al. 2006 and Katoh et al. 2005) and with much lower frequency among Manchus[19] (Xue et al. 2006, Katoh et al. 2005, and Karafet et al. 2001), Hezhe people,[10] Daurs,[10] Evenks,[9] Sibes (Xue et al. 2006), Kham Tibetans,[20] and Hui.[21] In a study of various populations of Hunan, O1b2-M176 was found in 0.55% (5/903) of all samples; specifically, this haplogroup was observed in 3.0% (1/33) of a sample of Iu Mien from Hunan, 1.9% (2/103) of a sample of Gàn Chinese from Hunan, 1.4% (1/71) of a sample of Kam from Hunan, and 1.1% (1/95) of a sample of Xong Miao from Hunan.[22] In a study published in July 2020, Y-DNA belonging to haplogroup O1b2-M176 was observed in 1.31% (4/305) of a sample of Han Chinese from Zibo, Shandong and in 1.06% (6/565) of a sample of Han Chinese from Zhaotong, Yunnan.[23]

Mitsuru Sakitani suggests that haplogroup O1b2, which is common in today Koreans, Japanese and Manchu, are one of the carriers of Liao civilization or Yangtze civilization. As the Liao civilization and the Yangtze civilization declined several tribes crossed westward and northerly, to the Korean Peninsula and the Japanese archipelago. However, Mitsuru Sakitani said that Currently, very little o1b2 are detected in the Yangtze River region, there are many problems in the theory that originate from the Yangtze River area.[24][25][26] Another study calls the haplogroup O1b1 as the major Austroasiatic paternal lineage and the haplogroup O1b2 (of Koreans and Japanese) as the "para-Austroasiatic" paternal lineage.[27]

Paragroup O-M176*

Y-DNA that belongs to O-M176(xK10, F3356) has been found in an individual from Hiroshima,[3] an individual from Fukushima,[3] an individual from Beijing,[3] and 1% (7/706) of a sample of males collected in Seoul and Daejeon.[28]

O-M176(x47z) has been found in approximately 3.5%[29] to 9.9%[30] of Japanese males. However, most of those individuals probably belong to subclades of O-K10(x47z).

O-K10

The majority of extant members of O-M176 belong to the subclade O-K10 (aka O-F3356 aka O-F1204). O-K10 (TMRCA 7,900 [95% CI 5,624 <-> 9,449] ybp according to Karmin et al. 2022, TMRCA 7,000 [95% CI 6,100 <-> 8,000] ybp according to YFull, TMRCA 6,980 years according to 23mofang) subsumes the prolific subclades O-47z, which occurs with especially high frequency in Japan, and O-L682, which occurs with especially high frequency in Korea, in addition to the relatively rare subclades O-CTS10687, which has been found in Japan, Korea, and China, and O-K3, which has been found among Han Chinese mostly in South Central China. O-L682 and O-K3 are linked by 18 SNPs that define the O-K4 clade, and thus their members are more closely related to one another by paternal lineage than any of them is related to any member of O-47z or O-CTS10687.

O-F3356(x47z, L682) has been found in 2% (14/706) of a sample of Koreans collected in Seoul and Daejeon, South Korea.[28] However, the status of these individuals' Y-DNA in regard to K4, K3, CTS10687, and phylogenetically equivalent SNPs has not been published.

O-CTS10687 has been found in 1.8% (1/56) of the JPT sample of Japanese from Tokyo, Japan.(Poznik et al. 2016)[3]

O-47z

Haplogroup O-47z
O1b2a1a1-CTS713(47z)
Possible time of origin7,870 [95% CI 5,720–12,630] years ago (Hammer et al. 2006)

7,100 [95% CI 6,100 <-> 8,300] ybp[3]
Possible place of originJapanese Archipelago (Hammer et al. 2006) or Korean Peninsula (Jin et al. 2003)
AncestorO-M176
Defining mutations47z
Highest frequenciesJapanese, Ryukyuans, Koreans, Manchus

O-47z or O-CTS11986 is a subclade of O-K10. It is found with high frequency among the Japanese and Ryukyuan populations of Japan, and with lower frequency among Koreans.

Haplogroup O-47z has been detected in approximately 24% of males who speak a Japonic language, while it has not been found at all among Ainu males whose Y-DNA has been tested in two genetic studies (Tajima et al. 2004, n=16; Hammer et al. 2006, n=4). Based on the STR haplotype diversity within Haplogroup O-47z, it has been estimated in a study published in 2006 that this haplogroup has expanded from a single founder who has lived approximately 3,810 (95% CI 1,640 <–> 7,960) years before present in a model according to which continuous, pure exponential population growth is assumed.[9] In a paper published in 2016, the time to most recent common ancestor of a set of fifteen members of the O-47z clade, all from the JPT (Japanese in Tokyo, Japan) sample of the 1000 Genomes Project, was estimated to be 4,500 years using a relatively slow mutation rate (μ = 0.76 x 10−9 per bp per year as according to Qiaomei Fu et al. 2014) or 3,900 years using a relatively fast mutation rate (μ = 0.888 x 10−9 per bp per year as according to A. Helgason et al. 2015).[29] Haplogroup O-47z also has been found among samples of modern Koreans, though with low frequency in comparison to both the frequency of O-47z in samples of Japanese and the frequency of O-M176(x47z) in samples of Koreans.[4]

O-K4

O-K4 is a subclade of O-K10. It includes at least two subclades, O-L682 and O-K3, which have been estimated to share a most recent common ancestor approximately 6,000 (95% CI 4,900 <-> 7,100) years before present,[3] 6,010 years before present,[2] or 6,327 (95% CI 4,575 <-> 7,762) years before present.[1]

O-K3
Haplogroup O-F940
Possible time of origin6,010 ybp[2]
Coalescence age2,650 years[2]
AncestorO-F2868
Defining mutationsCTS12145, F1912, F2206, F2703, F940, K3
Highest frequenciesHan Chinese (Hunan 0.79%, Guangxi, Chongqing, Hubei 0.25%, Jiangxi, Sichuan 0.17%, etc.[2])

The O-K3 (or O-F940) lineage is a subclade of O-K4 that has been observed in three individuals from Hunan,[3] one individual from Jiangxi,[3] one individual from Shaanxi,[3] and one individual from Henan.[15] The TMRCA of the three individuals from Hunan plus the singletons from Jiangxi and Shaanxi has been estimated to be 1,250 (95% CI 750 <-> 1,950) ybp.[3]

The aforementioned individuals (except the one from Henan, whose status is unknown) are all known to share the MF61543 and CTS2403 SNPs (among others) besides the F940 and K3 SNPs. According to 23mofang, O-MF61543 is found especially in Hunan and with lower frequency in surrounding parts of south-central China and has an estimated TMRCA of 1,580 years. Other branches of O-F940 are extremely rare and have been found sporadically in individuals from various locations across northern China, with one individual from as far south as Xuzhou in the east and another from as far south as Zigong in the west.[2]

O-L682
Haplogroup O-L682
O1b2a1a2a-L682
Possible time of origin6,327 [95% CI 4,575 <-> 7,762] ybp[1]
Possible place of originKorean Peninsula or Manchuria
AncestorO-M176, O-F3356
Defining mutationsL682
Highest frequenciesKoreans, Hezhen, Udege, Japanese, Ryukyuans, Manchus

The O-L682 subclade of O-K4 is believed to be related to Native Korean population. One study has found O-L682 Y-DNA in 19% (134/706) of Koreans sampled in Seoul and Daejeon.[28] O-L682 also has been found in Japanese in Tokyo, Okayama, Kōchi, and the US, Chinese in Liaoning and Shanxi, Shandong, and Beijing,[3] and Nanai people in China. Its descendants appear to have begun rapidly increasing in number at approximately the same time as those of its distant cousin O-47z, perhaps 4,000 years ago.[3]

Phylogenetics

Phylogenetic history

Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.

YCC 2002/2008
(Shorthand)
(α) (β) (γ) (δ) (ε) (ζ) (η) YCC 2002
(Longhand)
YCC 2005
(Longhand)
YCC 2008
(Longhand)
YCC 2010r
(Longhand)
ISOGG 2006 ISOGG 2007 ISOGG 2008 ISOGG 2009 ISOGG 2010 ISOGG 2011 ISOGG 2012
O-M17526VII1U28Eu16H9IO*OOOOOOOOOO
O-M11926VII1U32Eu16H9HO1*O1aO1aO1aO1aO1aO1aO1aO1aO1aO1a
O-M10126VII1U32Eu16H9HO1aO1a1O1a1aO1a1aO1a1O1a1O1a1aO1a1aO1a1aO1a1aO1a1a
O-M5026VII1U32Eu16H10HO1bO1a2O1a2O1a2O1a2O1a2O1a2O1a2O1a2O1a2O1a2
O-P3126VII1U33Eu16H5IO2*O2O2O2O2O2O2O2O2O2O2
O-M9526VII1U34Eu16H11GO2a*O2aO2aO2aO2aO2aO2aO2aO2aO2a1O2a1
O-M8826VII1U34Eu16H12GO2a1O2a1O2a1O2a1O2a1O2a1O2a1O2a1O2a1O2a1aO2a1a
O-SRY46520VII1U35Eu16H5IO2b*O2bO2bO2bO2bO2bO2bO2bO2bO2bO2b
O-47z5VII1U26Eu16H5IO2b1O2b1aO2b1O2b1O2b1aO2b1aO2b1O2b1O2b1O2b1O2b1
O-M12226VII1U29Eu16H6LO3*O3O3O3O3O3O3O3O3O3O3
O-M12126VII1U29Eu16H6LO3aO3aO3a1O3a1O3a1O3a1O3a1O3a1O3a1O3a1aO3a1a
O-M16426VII1U29Eu16H6LO3bO3bO3a2O3a2O3a2O3a2O3a2O3a2O3a2O3a1bO3a1b
O-M15913VII1U31Eu16H6LO3cO3cO3a3aO3a3aO3a3O3a3O3a3aO3a3aO3a3aO3a3aO3a3a
O-M726VII1U29Eu16H7LO3d*O3cO3a3bO3a3bO3a4O3a4O3a3bO3a3bO3a3bO3a2bO3a2b
O-M11326VII1U29Eu16H7LO3d1O3c1O3a3b1O3a3b1-O3a4aO3a3b1O3a3b1O3a3b1O3a2b1O3a2b1
O-M13426VII1U30Eu16H8LO3e*O3dO3a3cO3a3cO3a5O3a5O3a3cO3a3cO3a3cO3a2c1O3a2c1
O-M11726VII1U30Eu16H8LO3e1*O3d1O3a3c1O3a3c1O3a5aO3a5aO3a3c1O3a3c1O3a3c1O3a2c1aO3a2c1a
O-M16226VII1U30Eu16H8LO3e1aO3d1aO3a3c1aO3a3c1aO3a5a1O3a5a1O3a3c1aO3a3c1aO3a3c1aO3a2c1a1O3a2c1a1

Original research publications

The following research teams per their publications were represented in the creation of the YCC Tree.

Phylogenetic trees

This phylogenetic tree of haplogroup O subclades is based on the YCC 2008 tree (Karafet et al. 2008) and subsequent published research.

  • O1b2 (IMS-JST022454, L272.2, M176/Page63/SRY465, M302, P49, F1942/Page92)
    • O1b2a (F1942/Page92)
      • O1b2a1 (CTS9259)
        • O1b2a1a (F3356)
          • O1b2a1a1 (47z, CTS713, CTS11986)
          • O1b2a1a2 (F2868, F3110, K4)
            • O1b2a1a2a (L682)
            • O1b2a1a2b (F940, F1912, F3390)
          • O1b2a1a3 (CTS10687, F1813, F1800)
        • O1b2a1b (CTS562)
      • O1b2a2 (Page90)

Table of frequencies of O-M176

Population Frequency Sample Size SNPs Source
Korean (Gangwon)0.39763M176(x47z)=20
47z=5
Kim et al. 2011
Korean
(National Biobank of Korea)
0.377300M176(x47z)=88
47z=25
Park 2013
South Korea0.37375M176/P49(x47z)=25
47z=3
Hammer et al. 2006
Japanese (Shizuoka)0.3446147z=13
M176/P49(x47z)=8
Hammer et al. 2006
Korean (Daejeon)0.338133M176(x47z)=30
47z=15
Park 2012
Japanese0.33526347z=66
M176/JST022454(x47z)=22
Nonaka, Minaguchi & Takezaki 2007
Korean (Jeju)0.32287M176(x47z)=20
47z=8
Kim et al. 2011
Japanese (Kyushu)0.3215347z=15
M176/P49(x47z)=2
Hammer et al. 2006
Korean (Seoul)0.316573M176(x47z)=125
47z=56
Park 2012
Korean (Jeolla)0.31190M176(x47z)=21
47z=7
Kim et al. 2011
Japanese (Aomori)0.3082647z=7
M176/P49(x47z)=1
Hammer et al. 2006
Korean (Chungcheong)0.30672M176(x47z)=15
47z=7
Kim et al. 2011
Japanese (Tokushima)0.3007047z=17
M176/P49(x47z)=4
Hammer et al. 2006
Korean (Gyeongsang)0.29884M176(x47z)=15
47z=10
Kim et al. 2011
Japanese0.29315747z=38
M176(x47z)=8
Kim et al. 2011
Korean (Seoul/Gyeonggi)0.282110M176(x47z)=23
47z=8
Kim et al. 2011
Korean (PRC)0.28025M176(x47z)=5
47z=2
Xue et al. 2006
Korean (Korea)0.27943M176(x47z)=6
47z=6
Xue et al. 2006
Japanese0.2774747z=11
M176(x47z)=2
Xue et al. 2006
Manchurians0.2714847z=9
M176(x47z)=4
Jin, Kim & Kim 2010
Korean (Seoul & Daejeon)0.269216M176(x47z)=37
47z=21
Kim et al. 2007
Japanese0.26210747z=21
M176(x47z)=7
Jin, Kim & Kim 2010
Okinawa0.2224547z=5
M176/P49(x47z)=5
Hammer et al. 2006
Korean0.201154M176(x47z)=22
47z=9
Jin, Kim & Kim 2010
Udeges0.09521M176(x47z)=2Jin, Kim & Kim 2010
Han (Beijing)0.02051M176(x47z)=1Kim et al. 2011
Manchu0.05735M176(x47z)=2Xue et al. 2006
Uriankhai (Mongolia)0.05060M176=3Katoh et al. 2005
Mongol (NE Mongolia)0.05020M176=1Di Cristofaro et al. 2013
Hezhe (PRC)0.04445M176(x47z)=2Xue et al. 2006
Manchu0.03852M176/P49(x47z)=2Hammer et al. 2006
Zakhchin (Mongolia)0.03360M176=2Katoh et al. 2005
Manchurian0.03330M176(x47z)=1Kim et al. 2011
Hakka (Taiwan)0.02934M176=1Trejaut et al. 2014
Buryat0.02836M176(x47z)=1Kim et al. 2011
Nanai
(Samar from Khabarovsk)
≤0.02737O-P31=1Bogunov et al. 2015
Daur0.02639M176(x47z)=1Xue et al. 2006
Evenk (PRC)0.02441M176/P49(x47z)=1Hammer et al. 2006
Xibe0.02441M176(x47z)=1Xue et al. 2006
Buryat0.02050M176(x47z)=1Jin, Kim & Kim 2010
Mongols (Mongolia)0.006160M176=1Di Cristofaro et al. 2013
Han (Taiwan)0.004258M176=1Trejaut et al. 2014
Zhuang0.00020M176/P49=0Hammer et al. 2006
Oroqen0.00022M176/P49=0Hammer et al. 2006
Hanoi, Vietnam0.00024M176=0Trejaut et al. 2014
Kalimantan0.00025M176=0Trejaut et al. 2014
Evenk (PRC)0.00026M176=0Xue et al. 2006
Sumatra0.00026M176=0Trejaut et al. 2014
Akha (Thailand)0.00027M176=0Trejaut et al. 2014
Alor0.00028M176=0Karafet et al. 2010
Han (Lanzhou)0.00030M176=0Xue et al. 2006
Even0.00031M176/P49=0Hammer et al. 2006
Oroqen0.00031M176=0Xue et al. 2006
Uyghur (Ürümqi)0.00031M176=0Xue et al. 2006
Han (Yili)0.00032M176=0Xue et al. 2006
Malay0.00032M176/P49=0Hammer et al. 2006
Australian aborigines0.00033M176/P49=0Hammer et al. 2006
Qiang0.00033M176=0Xue et al. 2006
Han (Chengdu)0.00034M176=0Xue et al. 2006
Hani (PRC)0.00034M176=0Xue et al. 2006
Li0.00034M176=0Xue et al. 2006
She0.00034M176=0Xue et al. 2006
Buyi0.00035M176=0Xue et al. 2006
Han (Harbin)0.00035M176=0Xue et al. 2006
Han (Meixian)0.00035M176=0Xue et al. 2006
Hui (PRC)0.00035M176=0Xue et al. 2006
Tibetan0.00035M176=0Xue et al. 2006
Yao (Bama)0.00035M176=0Xue et al. 2006
Yao (Liannan)0.00035M176=0Xue et al. 2006
Batak Toba (Sumatra)0.00038M176=0Karafet et al. 2010
Uyghur (Yili)0.00039M176=0Xue et al. 2006
East Indonesia0.00040M176=0Trejaut et al. 2014
Han (Guangdong)0.00040M176/P49=0Hammer et al. 2006
Yi (Butuo, Sichuan)0.00043M176/P49=0Hammer et al. 2006
Northern Han0.00044M176/P49=0Hammer et al. 2006
Khalkh0.00045M176=0Kim et al. 2011
Mongol (Inner Mongolia)0.00045M176=0Xue et al. 2006
Papua New Guinea0.00046M176/P49=0Hammer et al. 2006
Khalkh0.00048M176=0Jin, Kim & Kim 2010
Philippines0.00048M176/P49=0Hammer et al. 2006
Taiwanese aborigines0.00048M176/P49=0Hammer et al. 2006
Tujia0.00049M176/P49=0Hammer et al. 2006
She0.00051M176/P49=0Hammer et al. 2006
Melanesia0.00053M176/P49=0Hammer et al. 2006
Mandar (Sulawesi)0.00054M176=0Karafet et al. 2010
Han (Fujian)0.00055M176=0Trejaut et al. 2014
Indonesia (East)0.00055M176/P49=0Hammer et al. 2006
Miao0.00058M176/P49=0Hammer et al. 2006
Han (Yunnan)0.00060M176=0Kim et al. 2011
Minnan (Taiwan)0.00060M176=0Trejaut et al. 2014
Nias0.00060M176=0Karafet et al. 2010
Polynesia0.00060M176/P49=0Hammer et al. 2006
Yao0.00060M176/P49=0Hammer et al. 2006
Java0.00061M176=0Karafet et al. 2010
Filipino0.00064M176=0Kim et al. 2011
Mongol (Outer Mongolia)0.00065M176=0Xue et al. 2006
Uyghur0.00067M176/P49=0Hammer et al. 2006
Mentawai0.00074M176=0Karafet et al. 2010
Thailand0.00075M176=0Trejaut et al. 2014
Buryat0.00081M176/P49=0Hammer et al. 2006
Han (Taiwan)0.00084M176/P49=0Hammer et al. 2006
Borneo0.00086M176=0Karafet et al. 2010
Sri Lanka0.00091M176/P49=0Hammer et al. 2006
Lembata0.00092M176=0Karafet et al. 2010
Evenk (Russia)0.00095M176/P49=0Hammer et al. 2006
Altai0.00098M176/P49=0Hammer et al. 2006
Tibet0.000105M176/P49=0Hammer et al. 2006
Java0.000141M176=0Trejaut et al. 2014
Philippines0.000146M176=0Trejaut et al. 2014
Mongolia0.000149M176/P49=0Hammer et al. 2006
Sumba0.000350M176=0Karafet et al. 2010
Taiwan mountain tribes0.000355M176=0Trejaut et al. 2014
Taiwan plains tribes0.000370M176=0Trejaut et al. 2014
Flores0.000394M176=0Karafet et al. 2010
India0.000405M176/P49=0Hammer et al. 2006
Bali0.000641M176=0Karafet et al. 2010

See also

Genetics

Y-DNA O subclades

Y-DNA backbone tree

References

Footnotes

  1. 256/800=32.0% O-M176 in a pool of all Japanese samples of (Xue et al. 2006), (Katoh et al. 2005), (Jin, Kim & Kim 2010), (Nonaka, Minaguchi & Takezaki 2007), (Poznik et al. 2016), and all non-Ainu and non-Okinawan Japanese samples of (Hammer et al. 2006).
  2. 202/677=29.8% O-M176 in a pool of all ethnic South Korean samples of (Hammer et al. 2006), (Xue et al. 2006), (Katoh et al. 2005), (Kim et al. 2007), and (Park 2013)
  3. 30/132=22.7% O-M176 in a pool of all Okinawan data from (Hammer et al. 2006) and (Nonaka, Minaguchi & Takezaki 2007)
  4. 30/123=24.3% O-M176 in a pool of all ethnic North Korea samples of (Jeong 2018)
  5. 150/628=23.9% O-47z in a pool of all non-Ainu and non-Okinawan Japanese samples of (Jin et al. 2003), (Hammer et al. 2006), (Xue et al. 2006), and (Nonaka, Minaguchi & Takezaki 2007)
  6. 22/132=16.7% O-47z in a pool of all Okinawan samples of (Hammer et al. 2006) and (Nonaka, Minaguchi & Takezaki 2007)
  7. 41/519=7.9% O-47z in a pool of all ethnic Korean samples of (Jin et al. 2003), (Hammer et al. 2006), (Xue et al. 2006), and (Kim et al. 2007)
  8. 9/135=6.7% O-47z in a pool of all "Manchu" or "Manchurian" samples of (Hammer et al. 2006), (Xue et al. 2006), and (Jin, Kim & Kim 2010)
  9. 41/519=7.9% O-L682 in a pool of all ethnic Korean samples of (Yoo 2014), (Katoh et al. 2005), and (Kim et al. 2011)
  10. 22/132=16.7% O-47z in a pool of all Okinawan samples of (Hammer et al. 2006) and (Nonaka, Minaguchi & Takezaki 2007)
  11. 150/628=23.9% O-47z in a pool of all non-Ainu and non-Okinawan Japanese samples of (Jin et al. 2003), (Hammer et al. 2006), (Xue et al. 2006), and (Nonaka, Minaguchi & Takezaki 2007)
  12. 9/135=6.7% O-47z in a pool of all "Manchu" or "Manchurian" samples of (Hammer et al. 2006), (Xue et al. 2006), and (Jin, Kim & Kim 2010)

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Sources

Further reading

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