rs3761863

A SNP in the LOC105369736 gene on chromosome 12. Its most notable genotype is T;T: common in clinvar

Gene
LOC105369736
Location
Chr 1240,364,850 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
45%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in clinvarTypical · 0.024% of people

SNPedia records rs3761863 on the minus strand: (A;A). 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.

  • AverageT;T 24%
  • European ancestry (Utah)T;T 13%
  • Han Chinese (Beijing)T;T 31%
  • Japanese (Tokyo)T;T 35%
  • Yoruba (Nigeria)T;T 29%
  • African ancestry (Southwest US)T;T 19%
  • Chinese (Denver)T;T 24%
  • Gujarati IndianT;T 15%
  • Luhya (Kenya)T;T 31%
  • Mexican ancestry (Los Angeles)T;T 33%
  • Maasai (Kenya)T;T 17%
  • TuscanT;T 12%

Other LOC105369736 SNPs

All LOC105369736 SNPs

Source and license

Adapted from rs3761863 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.