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Haplogroup R1b

Haplogroup R1b (Y-DNA).jpg

Time of origin less than 18,500 years BP[1]
Place of origin Western Asia [2]
Ancestor R1
Descendants R1b1a (R-V88), R1b1b (R-P297)
Defining mutations 1. M343 defines R1b in the broadest sense
2. P25 defines R1b1, making up most of R1b, and is often used to test for R1b
3. In some cases, major downstream mutations such as M269 are used to identify R1b, especially in regional or out-of-date studies
Highest frequencies Western Europe, Northern Cameroon, Hazara, Bashkirs
Haplogroup R1b Distribution

In human genetics, Haplogroup R1b is the most frequently occurring Y-chromosome haplogroup in Western Europe, Bashkortostan[3] and in parts of sub-Saharan Central Africa (for example around Chad and Cameroon). R1b is also present at lower frequencies throughout Eastern Europe, Western Asia, Central Asia, parts of North Africa. Due to European emigration it also reaches high frequencies in the Americas and Australia. While Western Europe is dominated by the R1b1b2 (R-M269) branch of R1b, the Chadic-speaking area in Africa is dominated by the branch known as R1b1a (R-V88). These represent two very successful "twigs" on a much bigger "family tree".



"R1b", "R1b1", and so on are "phylogenetic" or family tree based names which explain the branching of the family tree of R1b. For example R1b1a and R1b1b would be branches of R1b1, descending from a common ancestor. This means that these names can change with new discoveries.

The alternative way of naming haplogroups is to refer to the mutations used to define and identify them. Haplogroup R1b is now identified by the presence of the single-nucleotide polymorphism (SNP) mutation M343, which was discovered in 2004.[4] From 2002 to 2005, R1b was defined by the presence of SNP P25.

Standardized naming as described above, both using phylogenetic or mutational systems, was first proposed in 2002 by the Y Chromosome Consortium. Prior to 2002, today's Haplogroup R1b had a number of names in differing nomenclature systems, such as Hg1 and Eu18.[5]

Since 2002, a major update of the YCC phylogenetic nomenclature was made in 2008 by Karafet et al. which took account of newer discoveries of branches which could be clearly defined by SNP mutations, including some which changed the understanding of R1b's family tree.[1] Since 2008 it has become increasing necessary to refer to the frequently updated listing made on the ISOGG website.[2]


R1b is a branch of the MNOPS "macro-haplogroup," which is one of the predominant groupings of all human male lines outside of Africa, and this whole group, along indeed with all of macro-haplogroup F, is believed to have originated in Asia.

Macro-haplogroup MNOPS

Haplogroup M. New Guinea, Melanesia, eastern Indonesia, and Polynesia.

Macro-haplogroup NO

Haplogroup N. Mainly found in North Asia and northeastern Europe.

Haplogroup O. Mainly found in East Asia, Southeast Asia, and Austronesia.

Macro-haplogroup P

Haplogroup Q. Mainly found in North Asia and the Americas.

Macro-haplogroup R
Macro-haplogroup R1

Haplogroup R1a. Mainly found in Eastern Europe, South Asia, and Central Asia.

Haplogroup R1b. Mainly found in Western Europe, Central Africa, and Central Asia.

Haplogroup R2. Mainly found in South Asia.

Haplogroup S. New Guinea, Melanesia, and eastern Indonesia.

It was initially believed that R1b, or at least the majority of it in Europe, dispersed from Iberia after the Last Glacial Maximum, and had only come from Asia much earlier. A variant of this idea was that there may have been two separate R1b dispersals in the Mesolithic period, one from Anatolia, and one from Iberia.[4] However, more recently it has become more widely accepted that R1b entered Europe from Asia more recently, perhaps in the Neolithic.[6][7]

In 2008 T. Karafet et al. estimated the age of R1 as 18,500 years before present.[1]

Root of R1b tree

The identifiers below are those from the 2010 revision of the ISOGG tree.[2]

still un-defined

R-M343* (R1b*)

still un-defined

R-P25* (R1b1*)


R1b1a (R-V88). Most common Sub-Saharan African R1b.

still un-defined

R-P297* (R1b1b*)


R-M73 (R1b1b1). Found in Central Asia.

still un-defined

R-M269* (R1b1b2*)


R-L23 (R1b1b2a). Most common European R1b

R1b* (that is R1b with no subsequent distinguishing SNP mutations) is extremely rare. Two cases were reported in a large study of Turkey.[4] In a study of Jordan it was found that no less than 20 out of all 146 men tested (13.7%), including most notably 20 out of 45 men tested from the Dead Sea area, were positive for M173 (R1) but negative for P25 and M269, mentioned above, as well as the R1a markers SRY10831.2 and M17.[8] Hassan et al. (2008) found an equally surprising 14 out of 26 (54%) of Sudanese Fulani who were M173+ and P25-.[9] Wood et al. report 2 Egyptian cases out of a sample of 1122 people from various African countries.[10] Such cases could possibly be either R1b* (R-M343*) or R1a* (R-M420*), demonstrating the importance of checking exact mutations tested when comparing findings in this field.

It is however possible that some of the rare examples represent a reversion of marker P25 from a positive back to a negative ancestral state.[11]

Ancient clades within R1b1 (R-P25)

An up-to-date compliation of data taking the latest information into account can be found in Cruciani et al. (2010) which can be summarised as follows[12]:-

Continent Population #No. Total% R1b1* (R-P25*) R1b1a (R-V88) R1b1b2 (R-M269) R1b1b1 (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 Italians 1173 26.6% 0.0% 0.2% 26.4% 0.0%
Europe Corsicans 141 48.9% 0.0% 0.7% 48.2% 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 Balkanians 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


R1b1*, like R1b* is rare. Examples are mentioned in older articles, for example two in a sample from Turkey.[4] Most cases, especially in Africa, are thought to be almost mostly in the more recently discovered sub-clade R-V88. Most or all examples of R1b therefore fall into subclades R1b1a (R-V88) or R1b1b (R-P297). Cruciani et al. in the large 2010 study found 3 cases amongst 1173 Italians, 1 out of 328 West Asians and 1 out of 156 East Asians.[12] Cases from older studies are discussed below as probable cases of R1b1a (R-V88).


R1b1a is defined by the presence of SNP marker V88, the discovery of which was announced in 2010 by Cruciani et al.[12] Apart from individuals in southern Europe and Western Asia, the majority of R-V88 was found in northern and central Africa:

Region Population Country Language N Total% R1b1a (R-V88) R1b1b2 (R-M269) R1b1a* (R-V88*) R1b1a4 (R-V69)
N Africa Composite Morocco AA 338 0.0% 0.3% 0.6% 0.3% 0.0%
N Africa Mozabite Berbers Algeria AA/Berber 67 3.0% 3.0% 0.0% 3.0% 0.0%
N Africa Northern Egyptians Egypt AA/Semitic 49 6.1% 4.1% 2.0% 4.1% 0.0%
N Africa Berbers from Siwa Egypt AA/Berber 93 28.0% 26.9% 1.1% 23.7% 3.2%
N Africa Baharia Egypt AA/Semitic 41 7.3% 4.9% 2.4% 0.0% 4.9%
N Africa Gurna Oasis Egypt AA/Semitic 34 0.0% 0.0% 0.0% 0.0% 0.0%
N Africa Southern Egyptians Egypt AA/Semitic 69 5.8% 5.8% 0.0% 2.9% 2.9%
C Africa Songhai Niger NS/Songhai 10 0.0% 0.0% 0.0% 0.0% 0.0%
C Africa Fulbe Niger NC/Atlantic 7 14.3% 14.3% 0.0% 14.3% 0.0%
C Africa Tuareg Niger AA/Berber 22 4.5% 4.5% 0.0% 4.5% 0.0%
C Africa Ngambai Chad NS/Sudanic 11 9.1% 9.1% 0.0% 9.1% 0.0%
C Africa Hausa Nigeria (North) AA/Chadic 10 20.0% 20.0% 0.0% 20.0% 0.0%
C Africa Fulbe Nigeria (North) NC/Atlantic 32 0.0% 0.0% 0.0% 0.0% 0.0%
C Africa Yorubad Nigeria (South) NC/Defoid 21 4.8% 4.8% 0.0% 4.8% 0.0%
C Africa Ouldeme Cameroon (Nth) AA/Chadic 22 95.5% 95.5% 0.0% 95.5% 0.0%
C Africa Mada Cameroon (Nth) AA/Chadic 17 82.4% 82.4% 0.0% 76.5% 5.9%
C Africa Mafa Cameroon (Nth) AA/Chadic 8 87.5% 87.5% 0.0% 25.0% 62.5%
C Africa Guiziga Cameroon (Nth) AA/Chadic 9 77.8% 77.8% 0.0% 22.2% 55.6%
C Africa Daba Cameroon (Nth) AA/Chadic 19 42.1% 42.1% 0.0% 36.8% 5.3%
C Africa Guidar Cameroon (Nth) AA/Chadic 9 66.7% 66.7% 0.0% 22.2% 44.4%
C Africa Massa Cameroon (Nth) AA/Chadic 7 28.6% 28.6% 0.0% 14.3% 14.3%
C Africa Other Chadic Cameroon (Nth) AA/Chadic 4 75.0% 75.0% 0.0% 25.0% 50.0%
C Africa Shuwa Arabs Cameroon (Nth) AA/Semitic 5 40.0% 40.0% 0.0% 40.0% 0.0%
C Africa Kanuri Cameroon (Nth) NS/Saharan 7 14.3% 14.3% 0.0% 14.3% 0.0%
C Africa Foulbe Cameroon (Nth) NC/Atlantic 18 11.1% 11.1% 0.0% 5.6% 5.6%
C Africa Moundang Cameroon (Nth) NC/Adamawa 21 66.7% 66.7% 0.0% 14.3% 52.4%
C Africa Fali Cameroon (Nth) NC/Adamawa 48 20.8% 20.8% 0.0% 10.4% 10.4%
C Africa Tali Cameroon (Nth) NC/Adamawa 22 9.1% 9.1% 0.0% 4.5% 4.5%
C Africa Mboum Cameroon (Nth) NC/Adamawa 9 0.0% 0.0% 0.0% 0.0% 0.0%
C Africa Composite Cameroon (Sth) NC/Bantu 90 0.0% 1.1% 0.0% 1.1% 0.0%
C Africa Biaka Pygmies CAR NC/Bantu 33 0.0% 0.0% 0.0% 0.0% 0.0%
W Africa Composite 123 0.0% 0.0% 0.0% 0.0% 0.0%
E Africa Composite 442 0.0% 0.0% 0.0% 0.0% 0.0%
S Africa Composite 105 0.0% 0.0% 0.0% 0.0% 0.0%
TOTAL 1822
still un-defined

R-M343* (R1b*)

still un-defined

R-P25* (R1b1*)

still un-defined

R-V88* (R1b1a*)


R-M18 (R1b1a1)


R-V8 (R1b1a2)


R-V35 (R1b1a3)


R-V69 (R1b1a4)

R-P297 (R1b1b)

As can be seen in the above data table, R1b1a is found in northern Cameroon in west central Africa at a very high frequency, where it is considered to be caused by a pre-Islamic movement of people from Eurasia.[13][10]

Suggestive results from other studies which did not test for the full range of new markers discovered by Cruciani et al. have also been reported, which might be in R-V88.

  • Wood et al. reported high frequencies of men who were R-P25 positive and M269 negative, amongst the same north Cameroon area where Cruciani et al. reported high R-V88 levels. However they also found such cases amongst 3% (1/32) of Fante from Ghana, 9% (1/11) of Bassa from southern Cameroon, 4% (1/24) of Herero from Namibia, 5% (1/22) of Ambo from Namibia, 4% (4/92) of Egyptians, and 4% (1/28) of Tunisians. [10]
  • Luis et al. found the following cases of men M173 positive (R1), but negative for M73 (R1b1b1), M269 (R1b1b2), M18 (R1b1a1, a clade with V88, M18 having been discovered before V88) and M17 (R1a1a): 1 of 121 Omanis, 3 of 147 Egyptians, 2 of 14 Bantu from southern Cameroon, and 1 of 69 Hutu from Rwanda.[14]


R1b1a1 is a sub-clade of R-V88 which is defined by the presence of SNP marker M18.[1] It has been found only at low frequencies in samples from Sardinia[15][16] and Lebanon.[17]


R1b1b is defined by the presence of SNP marker P297. In 2008 this polymorphism was recognised to combine M73 and M269 into one R1b1b cluster.[1] The majority of Eurasian R1b is within this clade, representing a very large modern population, which has been relatively well studied, therefore the branching within this clade can be explained in detail below.


R1b1c is defined by the presence of SNP marker M335. This haplogroup was created by the 2008 reorganisation of nomenclature and should not be confused with R1b1b2, which was previously called R1b1c. Its position in relation to the much more populous sub-clade R1b1b is uncertain.[1] The M335 marker was first published in 2004, when one example was discovered in Turkey, which was classified at that time as R1b4.[4]

Major clades within R1b1b (R-P297)


R1b1b1 is defined by the presence of SNP marker M73. It has been found at generally low frequencies throughout central Eurasia,[15] and with relatively high frequency among Hazaras in Pakistan (8/25 = 32%[18]) and among Bashkirs in Bashkortostan (62/471 = 13.2%), 44 of these being found among the 80 tested Bashkirs of the Abzelilovsky District in the Republic of Bashkortostan (55.0%).[19]


R1b1b2 is defined by the presence of SNP marker M269. It has been found at generally low frequencies throughout central Eurasia,[15] and with relatively high frequency among Bashkirs of the Bashkortostan and Perm region (84.0%).[20]

Long-hand: R1b1b2 (formerly R1b1c, R1b3)
Defining SNP: M269
Parent Clade: R-P297
Subclades: R-P311

This subclade is defined by the presence of the M269 marker. From 2003 to 2005 what is now R1b1b2 was designated R1b3. From 2005 to 2008 it was R1b1c.

still un-defined

R-M269* (R1b1b2*)

still un-defined

R-L23* (R1b1b2a*)

still un-defined

R-L51* (R1b1b2a1*)

still un-defined

R-P310/L11* (R1b1b2a1a*)


R-U106 (R1b1b2a1a1)


R-P312 (R1b1b2a1a2)

In articles published around 2000 it was proposed that this clade came into existence in Europe before the last Ice Age,[21] but more recently this scenario is no longer receiving much mainstream attention. A much newer estimate for R1b1b2 arising is around 5,000 to 8,000 years ago.[7] It also appears increasingly to be the case that Western European R1b is dominated by R-P310, also known as R-L11. It is this Western European branch which is in turn dominated by U106 and P312, and the typical most common STR Y DNA signature for Western Europe, the so-called Atlantic Modal Haplotype, which is also sometimes referred to as "Haplotype 15". Haplotype 15 is contrasted with "Haplotype 35", which has long been noted as a distinct type of R1b1b2, more common towards the southeast of Europe.

R1b1b2a1a1 (R-U106)

This subclade is defined by the presence of the marker U106, also known as S21 and M405. It appears to represent over 25% of R1b in Europe.

Long-hand: R1b1b2a1a/R1b1b2g/R1b1c9
Defining SNP: U106/S21/M405
Parent Clade: P310/S129
Subclades: U198/S29/M405, S26/L1/DYS439(null), L48/S162 (comprising L44, L45, L46, L47), L5, L6, P89.2, P107
still un-defined

R-U106* (R1b1b2a1a1*)


R-U198 (R1b1b2a1a1a)


R-S26 (R1b1b2a1a1c)


R-L48* (R1b1b2a1a1d*)


R-L47* (R1b1b2a1a1d1*)

R-L44 (R1b1b2a1a1d1a)

In Europe, the subclade (including its own subclades) has a distribution running north west to east and is found in higher concentrations in England (21.4%) and Scandinavia (Denmark 17.7%), reaches a maximum in the Netherlands (37.2%) and slopes down to the east through Germany (20.5%) and the Alps (Switzerland 13.3%, Austria 22.7%) towards the Czech Republic (13.9%) and Ukraine (9.4%). Towards North-Eastern Europe the concentration goes down to 8.2% in Poland and 7.2% in Russia. The subclade appears to be omnipresent in Europe, although it becomes less pronounced in Ireland (5.9%) and France (7.1%) and, further towards the Mediterranean, low values are measured in, Italy (3.5%), and Turkey (0.4%).[22] The frequency of this subclade remains unknown in certain parts of Europe such as Iberia and the Balkans.

The age of U106 is around 3,100-3,900 years old.[citation needed]

The exact technical definition of the SNP was not initially released for commercial reasons, but the same marker was subsequently independently identified (as their "U106").[23]

Craig Venter and James Watson, who in 2007 became the first two individuals to have their complete genomes published, both belong to this subclade.

Downstream of U106 are U198/S29/M467, P107, P89.2, L1/S26/DYS439(null), L5, L6, L48/S162 (with L47, which contains L44 - further subdivided in the L45, L46 and L164 subgroups; L148; L179; and L188), L127.2 and L199.


This subclade is defined by the presence of the marker U198, also known as S29 and M467. Although attested in southern England and Germany in the region previously inhabited by the Saxons, it is unknown if this marker arrived in England with the Anglo-Saxons in the 5th Century. Only low values of the marker have been detected over a wide area that besides England (1.4%) and Germany (1.8%) includes the Netherlands (maximum value 2.1%), Denmark (0.9%) and Russia (1.8%).[22] The age of U198 is around 2-3,000 years.


This subclade is defined by the presence of the marker L1/S26/DYS439(null). It occurs in less than half of a percent of R1b males, mainly with roots in the south and east of England and in Germany. L1, first discovered by Family Tree DNA, then confirmed and named S26 by EthnoAncestry,[24] is located in the flanking region of DYS439, and when it occurs, it inhibits the FTDNA primers from binding, thus producing an apparent null allele or null439.[25]


This subclade is defined by the presence of the marker L48/S162 and is also known as R1b1b2a1a4 (by Family Tree DNA - FTDNA). It is the largest subclade of R1b1b2a1a1. As of January 23, 2010, based on FTDNA tests of samples from 455 people, L48 was detected in 267, or 58.0% of those tested. Based on May 2009 results, from among those with L48+ results at that time, 90% had DYS390 of 23 or less, while 10% a value of 24 or more. Among those tested L48-, 16% had DYS390 of 23 or less, while 84% a value of 24 or more. Therefore, there seems to be a correlation between values of 23 or lower for DYS390 and L48+, among those tested U106+.[26] The age of L48 is around 2,900-3,100 years old.

R1b1b2a1a1d has a subclade R1b1b2a1a1d1 (defined by the marker L47), which in turn, seems to be including subclades R1b1b2a1a1d1*, R1b1b2a1a1d1a defined by the marker L44. Furthermore, L44 comprises L45, L46, L164 and L237.[27]

As of January 23, 2010, based on FTDNA tests of samples from the R1b-U106 project, there were 87 published test results (including Craig Venter's) for L47, with 21 positive (24.1%), including 13 persons originated from the United Kingdom, one person from Picardy, France and one Ashkenazi person of probable Sephardic origin (so called Iberian Ashkenazim) from Belarus[28]. As well, due to the genetic distances among the members so far L47+, the age of this cluster is probably quite old, perhaps 2,700-2,900 years[citation needed]. It is possible that L47 emerged not too long after the L48 "parent" cluster. Preliminary data would strongly suggest that the L48 SNP occurred only a short period of time after the U106 SNP occurred, likely 200 years or less[citation needed].

With limited data for L46+ haplotypes at this point, it would appear that the L47 SNP occurred only a short period of time after the L48 SNP occurred, likely 200 years or less. However, more results and proper statistical analysis will be required. So far, these are only observations based on a few initial results. Downstream of L47 is also rs9786514 A+, which defines a new sub-haplogroup of L147 ("R1b1b2a1a1d1b").

For the R1b1b2a1a1d1a defined by marker L44, as of January 23, 2010, based on FTDNA tests of samples from the R1b-U106 project, there were 59 test results for L44, with 6 positive (10.2%) and 53 negative. Downstream of L44, L46 has 56 test results, with 4 positive (7.1%) and 52 negative. As well, it is possible that L45 could be downstream of L44 and upstream of 46, but FTDNA has not started testing L45 yet. The age of L46 could be around 1,500 years before present (YBP)[citation needed].

R1b1b2a1a1d has another subclade defined by the marker L148. As of January 23, 2010, based on FTDNA tests of samples from the R1b-U106 project, there were 19 test results for L148, with 3 positive (15.8%) and 16 negative.[29]. FamilyTreeDNA's Houston Lab Director, Thomas Krahn, has posted a working YDNA tree showing potential new subclades, under R1b1b2a1a1d, defined by markers L179, L180, L188, L200, and M157.2.[30] Their frequency remains unknown.[31].

R1b1b2a1a2 (R-P312)

The P312 SNP appears to account for at least half of European R1b1b2. Although unpublished it was included in chip-based commercial DNA tests towards the end of 2007 and analysis of the first available results in early 2008 by amateur geneticists indicated it has a significant place in the Y-DNA tree. This led to rapid development of stand-alone tests by both EthnoAncestry and Family Tree DNA. The results from customers of these companies and testing of control samples for the rarer SNPs have confirmed the status of this SNP relative to the above list.

Long-hand: R1b1b2a1a2
Defining SNP: P312 (also called S116, rs34276300)
Parent Clade: R-P310
Subclades: R-M153, R-M167, R-U152, R-L21
still un-defined

R-P312* (R1b1b2a1a2*)


R-M65 (R1b1b2a1a2a)


R-M153 (R1b1b2a1a2b)


R-M167 (R1b1b2a1a2c)

still un-defined

R-U152* (R1b1b2a1a2d*)


R-L2* (R1b1b2a1a2d3*)

R-L20 (R1b1b2a1a2d3a)


R-L165/S68 (R1b1b2a1a2e)


R-L21* (R1b1b2a1a2f*)

R-M222 (R1b1b2a1a2f2)

R-L226/S168 (R1b1b2a1a2f4)


This subclade is defined by the presence of the marker R-M153. It has been found mostly in Basques and Gascons, among whom it represents a sizeable fraction of the Y-DNA pool[32][33][34], though is also found occasionally among Iberians in general. The first time it was located (Bosch 2001[35]) it was described as H102 and included 7 Basques and one Andalusian.


This subclade is defined by the presence of the marker R-M167/SRY2627. The first author to test for this marker (long before modern haplogroup nomenclature existed) was Hurles in 1999[36]. He found it relatively common among Basques (13/117: 11%) and Catalans (7/32: 22%). Other occurrences were found among other Spanish, Béarnais, other French, British and Germans.

In 2000 Rosser[37] also tested for that same marker, naming the haplogroup Hg22, and again it was found mainly among Basques (19%), in lower frequencies among French (5%), Bavarians (3%), Spanish (2%), Southern Portuguese (2%), and in single occurrences among Romanians, Slovenians, Dutch, Belgians and English.

In 2001 Bosch described this marker as H103, in 5 Basques and 5 Catalans.[35] Further regional studies have located it in significant amounts in Asturias, Cantabria and Galicia, as well as again among Basques.[38] Cases in the Azores and Latin America have also been reported. In 2008 two research papers by López-Parra[34] and Adams,[33] respectively, identified it as very important in all the Pyrenees, with some presence further south in Iberia (specially in the Eastern half but also in Northern Portugal). It is specially prevalent among Catalans, where it includes some 20% of all men.


This subclade is defined by the presence of the marker R-U152 also called S28[39]. Its discovery was announced in 2005 by EthnoAncestry[24] and subsequently identified independently by Sims et al. (2007).[40] Although sample sizes are relatively small, it appears to reach a maximum in Alpine Germany and Switzerland. The Iron Age La Tène culture originated in this area, but an association with R1b1b2a1a2d has yet to be demonstrated.

It is found from Greece westward to the Bay of Biscay in France, but the percentages here are much less than found in the Alps. It has yet to be found anywhere in Ireland or Spain[citation needed]. Northern Italy seems to be a meeting place for both U106 and U152.


This subclade is defined by the presence of the marker S68 which was reported by in 2007. It has been seen in an individual from Scotland and another from Sweden. This subclade is unlikely to be found in much more than 2% of the R1b population.[24] In Fall 2009 Family Tree DNA discovered the same SNP in and named it L165.


This subclade is defined by the presence of the marker L21. Early results suggest that it is common in Britain, Ireland and possibly northern France. It is also apparently common in Germany and Scandinavia, but is rare in Iberian or Italian male lines.


This subclade is defined by the presence of the marker M222. It is particularly associated with male lines which are Irish or Scottish. In this case, the relatively high frequency of this specific subclade among the population of certain counties in northwestern Ireland may be due to positive social selection, as it is suggested to have been the Y-chromosome haplogroup of the Uí Néill dynastic kindred of ancient Ireland.[41][42] However it is not restricted to the Uí Néill as it is also associated with the closely related Connachta dynasties, called the Uí Briúin and Uí Fiachrach.[43] In addition it is also found in southern Scotland and so is thus commonly referred to as the Northwest Irish/Lowland Scots Variety.


This subclade is defined by the presence of the marker L226/S168. Commonly referred to as Irish Type III, it is concentrated in central western Ireland and associated with the Dál gCais kindred.[44][45]


R1b reaches its highest frequency in Atlantic Europe. Results from studies with small sample sizes should be treated with caution until more thorough testing is completed.


  • In South Asia, R1b is present at 8% in Iranians,[78] 7.4% in Pakistanis (including 4.5% R1b1b1-M73 and 2.8% R1b1b2-M269), while it is almost not found in India (0.55% R1b1b2-M269).[18] Haplogroup R1b1b2-M269 has been found in approximately 11% of a sample of Newars in Nepal.[79]
  • In the Caucasus, haplogroup R1b may be found in 43% of Ossetian males[57] and in as many as 32.4% (238/734 P-92R7(xR1a1-SRY10831b))[80] to 36% (17/47 R1-M173(xR1a1a-M17))[64] of Armenians. It also has been found with lower frequency among Georgians (6/66 = 9.1% R1b1b2-M269[81] to 9/63 = 14.3% R1-M173(xR1a1a-M17)[82]) and Balkarians (2/38 = 5.3% R1b1-P25(xR1b1b2-M269) and 3/38 = 7.9% R1b1b2-M269 for a total of 5/38 = 13.2% R1b[81]).



Atlantic Modal Haplotype

A common haplotype within R1b is sometimes called the Atlantic Modal Haplotype, or haplotype 15. It reaches the highest frequencies in the Iberian Peninsula and in Great Britain and Ireland. In the Iberian Peninsula it reaches 70% in Portugal as a whole and more than 90% in NW Portugal, while the highest value is to be found among Spanish Basques. It was discovered prior to many of the SNPs now used to identify subclades of R1b and references to it can be found in some of the older literature. It corresponds most closely with subclade R1b1b2a1a [L11].

Haplotype 35

There also exists a haplotype associated with R1b1b2 characterized by DYS393=12 which is known in the literature as Haplotype 35 (ht35), or the Armenian Modal Haplotype.[citation needed]

Popular culture

Bryan Sykes, in his book Blood of the Isles, gives the populations associated with R1b the name of Oisín for a clan patriarch, much as he did for mitochondrial haplogroups in The Seven Daughters of Eve.

Stephen Oppenheimer also deals with this haplogroup in his book Origins of the British, giving the R1b clan patriarch the Basque name "Ruisko" in honour of what he thought was the Iberian origin of R1b.

See also

Human Y-chromosome DNA (Y-DNA) haplogroups (by ethnic groups · famous haplotypes)

most recent common Y-ancestor
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  • Luigi Luca Cavalli-Sforza (1994). The History and Geography of Human Genes. Princeton University Press.  ISBN 0-691-08750-4
  • Michel Morvan (1996) The linguistic origins of basque (in french), Bordeaux University Press. ISBN 2-86781-182-1

External links




Up to date as of February 01, 2010

From Familypedia

M343 is a genetic marker, announced in 2004, which defines a specific Y chromosome binary polymorphism. It now defines the Y chromosome haplogroup R1b (previously known as Hg1 and Eu18). This genetic marker is carried by most Western Europeans. It is carried by 70% of the entire population of England and 90% of some parts of Spain and Ireland and is also descended from the Cro-Magnon.

This marker is estimated to have originated in an individual male in Western Europe 30,000 or more years ago and has propagated since then to the population mentioned.

It also is said that Europeans with mutation M343 descended from ten men whose roots go back to mutation M9 somewhere on the Khirgan steppes when a great division of people went their own ways to the east, north and west.

The technical details of M343 are:

Nucleotide  change: C to A
Position (base pair): 402
Total size (base pairs):424
Forward 5′→3′: tttaacctcctccagctctgca
Reverse 5′→3′: acccccacatatctccagg 

This refers to a particular 424 base-pair fragment of DNA that the polymerase chain reaction produces when one uses the two "primer" strands listed.

M343 was announced in a group of 21 new Y-chromosome markers in

Human Genetics, Issue: Volume 114, Number 2
Date: January 2004, Pages: 127 - 148
Title: Excavating Y-chromosome haplotype strata in Anatolia
Authors: Cengiz Cinniolu, et al.

and has already been used in applications such as the Genographic Project. Note that M343 and M242 were the only two markers from this paper used by the Project.

See also

External links

This page uses content from the English language Wikipedia. The original content was at M343. The list of authors can be seen in the page history. As with this Familypedia wiki, the content of Wikipedia is available under the Creative Commons License.

This article uses material from the "M343" article on the Genealogy wiki at Wikia and is licensed under the Creative Commons Attribution-Share Alike License.


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