rs6809699

A SNP in the P2RY12 gene on chromosome 3. Its most notable genotype is A;A: common in clinvar

Gene
P2RY12
Location
Chr 3151,338,810 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
11%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.02% of people
  2. C;CGoodcommon on affy axiom dataTypical · 0.081% of people

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

Frequency

Share of each genotype in 9 HapMap populations.

  • AverageA;A 2% C;C 81%
  • European ancestry (Utah)A;A 3% C;C 66%
  • Han Chinese (Beijing)A;A 3% C;C 73%
  • Japanese (Tokyo)A;A <1% C;C 79%
  • Yoruba (Nigeria)A;A 0% C;C 100%
  • African ancestry (Southwest US)A;A 0% C;C 91%
  • Chinese (Denver)A;A 3% C;C 78%
  • Gujarati IndianA;A 1% C;C 81%
  • Mexican ancestry (Los Angeles)A;A 2% C;C 86%
  • TuscanA;A 2% C;C 79%

Conditions, medicines and genes

Other P2RY12 SNPs

All P2RY12 SNPs

Notes

From SNPedia

Notes

rs10935838, rs2046934, rs5853517, and rs6809699 venous thromboembolism lower risk of incident DVT/PE as compared to the reference haplotype H1 (odds ratio=0.50, 95% CI=0.27-0.93, p=0.028)

Source and license

Adapted from rs6809699 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.