rs643788

A SNP in the DPAGT1 gene on chromosome 11. Its most notable genotype is T;T: common in clinvar

Gene
DPAGT1
Location
Chr 11119,097,048 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
43%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in clinvarTypical · 0.034% of people

On SNPedia: (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.

  • AverageT;T 34%
  • European ancestry (Utah)T;T 25%
  • Han Chinese (Beijing)T;T 17%
  • Japanese (Tokyo)T;T 14%
  • Yoruba (Nigeria)T;T 54%
  • African ancestry (Southwest US)T;T 56%
  • Chinese (Denver)T;T 17%
  • Gujarati IndianT;T 25%
  • Luhya (Kenya)T;T 55%
  • Mexican ancestry (Los Angeles)T;T 38%
  • Maasai (Kenya)T;T 49%
  • TuscanT;T 27%

Other DPAGT1 SNPs

All DPAGT1 SNPs

Source and license

Adapted from rs643788 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.