rs34276300
A SNP on chromosome Y. Its most notable genotype is A;A: Paternal Haplogroup: R1b1b2a1a2
- Gene
- None listed
- Location
- Chr Y19,995,425 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
jogg.info Since R1b1c is very common, the first interesting discovery involved a SNP in that haplogroup, rs34276300, which was found to be ancestral in one branch of R1b1c and derived in several other branches. According to a 23andMe discussion, this is one of the SNPs that were re-analyzed in April 2009. Customers with older data may wish to redownload. SNPs affected: * rs4420638 * rs34276300 * rs3091244 * rs34601266 * rs2033003 * rs7900194 * rs9332239 * rs28371685 * rs1229984 * rs28399504.
Source and license
Adapted from rs34276300 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.