rs2639703
A SNP in the ENAH gene on chromosome 1. Its most notable genotype is A;A.
- Gene
- ENAH
- Location
- Chr 1225,625,209 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 41%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot ratedNo summary available.
- C;CNot rated1.6x risk
- C;TNot rated1.1x risk
- T;TNot ratednormal
On SNPedia: (A;A), (C;C), (C;T), (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.
- AverageA;A 0% C;C 23% C;T 45% T;T 32%
- European ancestry (Utah)A;A 0% C;C 7% C;T 42% T;T 51%
- Han Chinese (Beijing)A;A 0% C;C 8% C;T 32% T;T 60%
- Japanese (Tokyo)A;A 0% C;C 10% C;T 48% T;T 42%
- Yoruba (Nigeria)A;A 0% C;C 53% C;T 43% T;T 4%
- African ancestry (Southwest US)A;A 0% C;C 40% C;T 44% T;T 16%
- Chinese (Denver)A;A 0% C;C 11% C;T 46% T;T 43%
- Gujarati IndianA;A 0% C;C 37% C;T 47% T;T 17%
- Luhya (Kenya)A;A 0% C;C 46% C;T 46% T;T 7%
- Mexican ancestry (Los Angeles)A;A 0% C;C 16% C;T 47% T;T 38%
- Maasai (Kenya)A;A 0% C;C 22% C;T 58% T;T 21%
- TuscanA;A 0% C;C 8% C;T 44% T;T 48%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs2639703 has been reported in a large study to be associated with type-1 diabetes. The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.15 (CI 1.02-1.31), and for homozygotes, 1.61 (CI 1.31-1.99).
Source and license
Adapted from rs2639703 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.