Haplogroup R1b (Y-DNA) - R1b (R-M343) - R1b1a (R-P297) - R1b1a2 (R-M269)

R1b1a2 (R-M269)

R1b1a2 (2011 name) is defined by the presence of SNP marker M269. R1b1a2* or M269(xL23) is found at highest frequency in the central Balkans notably Kosovo with 7.9%, Macedonia 5.1% and Serbia 4.4%. Kosovo is notable in also having a high percentage of descendant L23* or L23(xM412) at 11.4% unlike most other areas with significant percentages of M269* and L23* except for Poland with 2.4% and 9.5% and the Bashkirs of southeast Bashkortostan with 2.4% and 32.2% respectively. Notably this Bashkir population also has a high percentage of M269 sister branch M73 at 23.4%. Five individuals out of 110 tested in the Ararat Valley, Armenia belonged to R1b1a2* and 36 to L23*, with none belonging to subclades of L23.

European R1b is dominated by R-M269. It has been found at generally low frequencies throughout central Eurasia, but with relatively high frequency among Bashkirs of the Perm Region (84.0%). This marker is also present in China and India at frequencies of less than one percent. The table below lists in more detail the frequencies of M269 in various regions in Asia, Europe, and Africa.

The frequency is about 71% in Scotland, 70% in Spain and 60% in France. In south-eastern England the frequency of this clade is about 70%; in parts of the rest of north and western England, Spain, Portugal, Wales and Ireland, it is as high as 90%; and in parts of north-western Ireland it reaches 98%. It is also found in North Africa, where its frequency surpasses 10% in some parts of Algeria.

From 2003 to 2005 what is now R1b1a2 was designated R1b3. From 2005 to 2008 it was R1b1c. From 2008 to 2011 it was R1b1b2.

M269
still un-defined

R-M269* (R1b1a2*)


L23
still un-defined

R-L23* (R1b1a2a*)


L150
still un-defined

R-L150* (R1b1a2a1*)


L51/M412
still un-defined

R-L51*/R-M412* (R1b1a2a1a*)


P310/L11
still un-defined

R-P310/L11* (R1b1a2a1a1*)


U106

R-U106 (R1b1a2a1a1a)


P312

R-P312 (R1b1a2a1a1b)





R-L277 (R1b1a1a1b)





As discussed above, in articles published around 2000 it was proposed that this clade been in Europe before the last Ice Age, but by 2010 more recent periods such as the European Neolithic have become the focus of proposals. A range of newer estimates for R1b1b2, or at least its dominant parts in Europe, are from 4,000 to a maximum of about 10,000 years ago, and looking in more detail is seen as suggesting a migration from Western Asia via southeastern Europe. Western European R1b is dominated by R-P310.

It was also in this period between 2000 and 2010 that it became clear that especially Western European R1b is dominated by specific sub-clades of R-M269 (with some small amounts of other types found in areas such as Sardinia). Within Europe, R-M269 is dominated by R-M412, also known as R-L51, which according to Myres et al. (2010) is "virtually absent in the Near East, the Caucasus and West Asia." This Western European population is further divided between R-P312/S116 and R-U106/S21, which appear to spread from the western and eastern Rhine river basin respectively. Myres et al. note further that concerning its closest relatives, in R-L23*, that it is "instructive" that these are often more than 10% of the population in the Caucasus, Turkey, and some southeast European and circum-Uralic populations. In Western Europe it is also present but in generally much lower levels apart from "an instance of 27% in Switzerland's Upper Rhone Valley." In addition, the sub-clade distribution map, Figure 1h titled "L11(xU106,S116)", in Myres et al. shows that R-P310/L11* (or as yet undefined subclades of R-P310/L11) occurs only in frequencies greater than 10% in Central England with surrounding areas of England and Wales having lower frequencies. This R-P310/L11* is almost non-existent in the rest of Eurasia and North Africa with the exception of coastal lands fringing the western and southern Baltic (reaching 10% in Eastern Denmark and 6% in northern Poland) and in Eastern Switzerland and surrounds.

In 2009, DNA extracted from the femur bones of 6 skeletons in an early-medieval burial place in Ergolding (Bavaria, Germany) dated to around 670 AD yielded the following results: 4 were found to be haplogroup R1b with the closest matches in modern populations of Germany, Ireland and the USA while 2 were in Haplogroup G2a.

Population studies which test for M269 have become more common in recent years, while in earlier studies men in this haplogroup are only visible in the data by extrapolation of what is likely. The following gives a summary of most of the studies which specifically tested for M269, showing its distribution in Europe, North Africa, the Middle East and Central Asia as far as China and Nepal.

Country Sampling sample R-M269 Source
Wales National 65 92.3% Balaresque et al. (2009)
Spain Basques 116 87.1% Balaresque et al. (2009)
Ireland National 796 85.4% Moore et al. (2006)
Spain Catalonia 80 81.3% Balaresque et al. (2009)
France Ille-et-Vilaine 82 80.5% Balaresque et al. (2009)
France Haute-Garonne 57 78.9% Balaresque et al. (2009)
England Cornwall 64 78.1% Balaresque et al. (2009)
France Loire-Atlantique 48 77.1% Balaresque et al. (2009)
France Finistère 75 76.0% Balaresque et al. (2009)
France Basques 61 75.4% Balaresque et al. (2009)
Spain East Andalucia 95 72.0% Balaresque et al. (2009)
Spain Castilla La Mancha 63 72.0% Balaresque et al. (2009)
France Vendée 50 68.0% Balaresque et al. (2009)
France Baie de Somme 43 62.8% Balaresque et al. (2009)
England Leicestershire 43 62.0% Balaresque et al. (2009)
Italy North-East (Ladin) 79 60.8% Balaresque et al. (2009)
Spain Galicia 88 58.0% Balaresque et al. (2009)
Spain West Andalucia 72 55.0% Balaresque et al. (2009)
Portugal South 78 46.2% Balaresque et al. (2009)
Italy North-West 99 45.0% Balaresque et al. (2009)
Denmark National 56 42.9% Balaresque et al. (2009)
Netherlands National 84 42.0% Balaresque et al. (2009)
Italy North East 67 41.8% Battaglia et al. (2008)
Russia Bashkirs 471 34.40% Lobov (2009)
Germany Bavaria 80 32.3% Balaresque et al. (2009)
Italy West Sicily 122 30.3% Di Gaetano et al. (2009)
Poland National 110 22.7% Myres et al. (2007)
Slovenia National 75 21.3% Battaglia et al. (2008)
Slovenia National 70 20.6% Balaresque et al. (2009)
Turkey Central 152 19.1% Cinnioğlu et al. (2004)
Republic of Macedonia National 64 18.8% Battaglia et al. (2008)
Italy East Sicily 114 18.4% Di Gaetano et al. (2009)
Crete National 193 17.0% King et al. (2008)
Italy Sardinia 930 17.0% Contu et al. (2008)
Iran North 33 15.2% Regueiro et al. (2006)
Moldova 268 14.6% Varzari (2006)
Greece National 171 13.5% King et al. (2008)
Turkey West 163 13.5% Cinnioğlu et al. (2004)
Romania National 54 13.0% Varzari (2006)
Turkey East 208 12.0% Cinnioğlu et al. (2004)
Algeria Northwest (Oran area) 102 11.8% Robino et al. (2008)
Russia Roslavl 107 11.2% Balanovsky et al. (2008)
Iraq National 139 10.8% Al-Zahery et al. (2003)
Nepal Newar 66 10.60% Gayden et al. (2007)
Serbia National 100 10.0% Belaresque et al. (2009)
Tunisia Tunis 139 7.2% Adams et al. (2008)
Algeria Algiers, Tizi Ouzou 46 6.5% Adams et al. (2008)
Bosnia-Herzegovina Serb 81 6.2% Marjanovic et al. (2005)
Iran South 117 6.0% Regueiro et al. (2006)
Russia Repievka 96 5.2% Balanovsky et al. (2008)
UAE 164 3.7% Cadenas et al. (2007)
Bosnia-Herzegovina Bosniak 85 3.5% Marjanovic et al. (2005)
Pakistan 176 2.8% Sengupta et al. (2006)
Russia Belgorod 143 2.8% Balanovsky et al. (2008)
Russia Ostrov 75 2.7% Balanovsky et al. (2008)
Russia Pristen 45 2.2% Balanovsky et al. (2008)
Bosnia-Herzegovina Croat 90 2.2% Marjanovic et al. (2005)
Qatar 72 1.4% Cadenas et al. (2007)
China 128 0.8% Sengupta et al. (2006)
India various 728 0.5% Sengupta et al. (2006)
Croatia Osijek 29 0.0% Battaglia et al. (2008)
Yemen 62 0.0% Cadenas et al. (2007)
Tibet 156 0.0% Gayden et al. (2007)
Nepal Tamang 45 0.0% Gayden et al. (2007)
Nepal Kathmandu 77 0.0% Gayden et al. (2007)
Japan 23 0.0% Sengupta et al. (2006)

Read more about this topic:  Haplogroup R1b (Y-DNA), R1b (R-M343), R1b1a (R-P297)