rs8017304

A SNP in the RAD51B gene on chromosome 14. Its most notable genotype is G;G: common in clinvar

Gene
RAD51B
Location
Chr 1468,318,360 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
48%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.031% of people

On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageG;G 31%
  • European ancestry (Utah)G;G 14%
  • Han Chinese (Beijing)G;G 35%
  • Japanese (Tokyo)G;G 30%
  • Yoruba (Nigeria)G;G 53%
  • African ancestry (Southwest US)G;G 42%
  • Chinese (Denver)G;G 34%
  • Gujarati IndianG;G 7%
  • Luhya (Kenya)G;G 46%
  • Mexican ancestry (Los Angeles)G;G 17%
  • Maasai (Kenya)G;G 38%
  • TuscanG;G 21%

Source and license

Adapted from rs8017304 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.