rs3847687

A SNP in the ADGRD1 gene on chromosome 12. Its most notable genotype is C;T: common in complete genomics

Gene
ADGRD1
Location
Chr 12131,040,508 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
30%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;TMost notableGoodcommon in complete genomicsTypical · 0.032% of people

SNPedia records rs3847687 on the minus strand: (A;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.

  • AverageC;T 32%
  • European ancestry (Utah)C;T 50%
  • Han Chinese (Beijing)C;T 26%
  • Japanese (Tokyo)C;T 18%
  • Yoruba (Nigeria)C;T 16%
  • African ancestry (Southwest US)C;T 37%
  • Chinese (Denver)C;T 24%
  • Gujarati IndianC;T 54%
  • Luhya (Kenya)C;T 23%
  • Mexican ancestry (Los Angeles)C;T 40%
  • Maasai (Kenya)C;T 33%
  • TuscanC;T 34%

Other ADGRD1 SNPs

All ADGRD1 SNPs

Source and license

Adapted from rs3847687 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.