rs966365

A SNP in the EDARADD gene on chromosome 1. Its most notable genotype is G;G: common in clinvar

Gene
EDARADD
Location
Chr 1236,394,471 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
23%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.011% of people
  2. A;AGoodcommon in complete genomicsTypical · 0.061% of people

SNPedia records rs966365 on the minus strand: (C;C), (T;T). 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 11% A;A 61%
  • European ancestry (Utah)G;G 6% A;A 71%
  • Han Chinese (Beijing)G;G 0% A;A 88%
  • Japanese (Tokyo)G;G 0% A;A 91%
  • Yoruba (Nigeria)G;G 25% A;A 24%
  • African ancestry (Southwest US)G;G 25% A;A 27%
  • Chinese (Denver)G;G <1% A;A 84%
  • Gujarati IndianG;G 0% A;A 93%
  • Luhya (Kenya)G;G 33% A;A 16%
  • Mexican ancestry (Los Angeles)G;G 0% A;A 78%
  • Maasai (Kenya)G;G 29% A;A 23%
  • TuscanG;G 3% A;A 73%

Source and license

Adapted from rs966365 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.