rs11650915

A SNP in the KRT12 gene on chromosome 17. Its most notable genotype is A;G.

Gene
KRT12
Location
Chr 1740,867,144 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
34%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableNot ratedNo summary available.Typical · 0.039% of people
  2. G;GGoodcommon in clinvarTypical · 0.048% of people

On SNPedia: (A;G), (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.

  • AverageA;G 39% G;G 48%
  • European ancestry (Utah)A;G 46% G;G 39%
  • Han Chinese (Beijing)A;G 50% G;G 21%
  • Japanese (Tokyo)A;G 50% G;G 15%
  • Yoruba (Nigeria)A;G 13% G;G 87%
  • African ancestry (Southwest US)A;G 30% G;G 70%
  • Chinese (Denver)A;G 56% G;G 14%
  • Gujarati IndianA;G 45% G;G 44%
  • Luhya (Kenya)A;G 14% G;G 85%
  • Mexican ancestry (Los Angeles)A;G 53% G;G 28%
  • Maasai (Kenya)A;G 22% G;G 74%
  • TuscanA;G 47% G;G 47%

Source and license

Adapted from rs11650915 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.