rs238238

A SNP in the ENO3 gene on chromosome 17. Its most notable genotype is A;A: common in clinvar

Gene
ENO3
Location
Chr 174,953,081 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
40%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.019% of people
  2. G;GNot ratedNo summary available.Typical · 0.033% of people

On SNPedia: (A;A), (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;A 19% G;G 33%
  • European ancestry (Utah)A;A 8% G;G 46%
  • Han Chinese (Beijing)A;A 34% G;G 14%
  • Japanese (Tokyo)A;A 36% G;G 13%
  • Yoruba (Nigeria)A;A 22% G;G 30%
  • African ancestry (Southwest US)A;A 11% G;G 38%
  • Chinese (Denver)A;A 44% G;G 15%
  • Gujarati IndianA;A 22% G;G 20%
  • Luhya (Kenya)A;A 13% G;G 36%
  • Mexican ancestry (Los Angeles)A;A 2% G;G 60%
  • Maasai (Kenya)A;A 16% G;G 40%
  • TuscanA;A 7% G;G 53%

Source and license

Adapted from rs238238 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.