rs3136516

A SNP in the F2 gene on chromosome 11. Its most notable genotype is G;G: common in clinvar

Gene
F2
Location
Chr 1146,739,206 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
31%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.061% 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 61%
  • European ancestry (Utah)G;G 21%
  • Han Chinese (Beijing)G;G 62%
  • Japanese (Tokyo)G;G 77%
  • Yoruba (Nigeria)G;G 99%
  • African ancestry (Southwest US)G;G 84%
  • Chinese (Denver)G;G 64%
  • Gujarati IndianG;G 39%
  • Luhya (Kenya)G;G 96%
  • Mexican ancestry (Los Angeles)G;G 31%
  • Maasai (Kenya)G;G 74%
  • TuscanG;G 23%

Other F2 SNPs

All F2 SNPs

Source and license

Adapted from rs3136516 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.