rs157582
A SNP in the TOMM40 gene on chromosome 19. Its most notable genotype is T;T: Weaker memory performance
- Gene
- TOMM40
- Location
- Chr 1944,892,962 (GRCh38)
- Highest magnitude
- 2.1Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 28%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableBadWeaker memory performance
- C;TNot ratedAverage memory performance
- C;CGoodStronger memory performance
SNPedia records rs157582 on the minus strand: (A;A), (A;G), (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.
- AverageT;T 10% C;T 38% C;C 52%
- European ancestry (Utah)T;T 6% C;T 35% C;C 58%
- Han Chinese (Beijing)T;T <1% C;T 40% C;C 59%
- Japanese (Tokyo)T;T 3% C;T 33% C;C 65%
- Yoruba (Nigeria)T;T 22% C;T 54% C;C 24%
- African ancestry (Southwest US)T;T 18% C;T 46% C;C 37%
- Chinese (Denver)T;T 5% C;T 23% C;C 73%
- Gujarati IndianT;T 6% C;T 23% C;C 71%
- Luhya (Kenya)T;T 30% C;T 52% C;C 18%
- Mexican ancestry (Los Angeles)T;T 3% C;T 36% C;C 60%
- Maasai (Kenya)T;T 19% C;T 47% C;C 35%
- TuscanT;T 2% C;T 29% C;C 69%
Related
Source and license
Adapted from rs157582 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.