rs2238472
A SNP in the ABCC6 gene on chromosome 16. Its most notable genotype is T;T: most likely a benign polymorphism
- Gene
- ABCC6
- Location
- Chr 1616,157,742 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 19%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableGoodmost likely a benign polymorphism
- C;TGoodmost likely a benign polymorphism
- C;CGoodcommon in clinvar
SNPedia records rs2238472 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 3% C;T 23% C;C 74%
- European ancestry (Utah)T;T 8% C;T 31% C;C 61%
- Han Chinese (Beijing)T;T <1% C;T 19% C;C 80%
- Japanese (Tokyo)T;T 4% C;T 27% C;C 68%
- Yoruba (Nigeria)T;T <1% C;T 14% C;C 85%
- African ancestry (Southwest US)T;T 2% C;T 19% C;C 79%
- Chinese (Denver)T;T <1% C;T 25% C;C 74%
- Gujarati IndianT;T 3% C;T 35% C;C 62%
- Luhya (Kenya)T;T 0% C;T 13% C;C 87%
- Mexican ancestry (Los Angeles)T;T 7% C;T 31% C;C 62%
- Maasai (Kenya)T;T <1% C;T 8% C;C 92%
- TuscanT;T 8% C;T 31% C;C 61%
Related
Source and license
Adapted from rs2238472 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.