rs8055236
A SNP in the CDH13 gene on chromosome 16. Its most notable genotype is G;G: common, but 2.2x higher risk for heart disease
- Gene
- CDH13
- Location
- Chr 1683,178,793 (GRCh38)
- Highest magnitude
- 1.7Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 24%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;ANot ratedNo summary available.
- G;GMost notableBadcommon, but 2.2x higher risk for heart disease
- G;TBad1.9x risk for heart disease
- T;TNot ratednormal
On SNPedia: (A;A), (G;G), (G;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% G;G 52% G;T 35% T;T 13%
- European ancestry (Utah)A;A 0% G;G 64% G;T 34% T;T 3%
- Han Chinese (Beijing)A;A 0% G;G 76% G;T 23% T;T 2%
- Japanese (Tokyo)A;A 0% G;G 72% G;T 27% T;T <1%
- Yoruba (Nigeria)A;A 0% G;G 19% G;T 47% T;T 34%
- African ancestry (Southwest US)A;A 0% G;G 25% G;T 46% T;T 30%
- Chinese (Denver)A;A 0% G;G 82% G;T 16% T;T 2%
- Gujarati IndianA;A 0% G;G 66% G;T 30% T;T 4%
- Luhya (Kenya)A;A 0% G;G 18% G;T 50% T;T 32%
- Mexican ancestry (Los Angeles)A;A 0% G;G 74% G;T 26% T;T 0%
- Maasai (Kenya)A;A 0% G;G 16% G;T 58% T;T 26%
- TuscanA;A 0% G;G 62% G;T 32% T;T 6%
Related
Conditions, medicines and genes
Other CDH13 SNPs
- rs1048612A;Acommon in clinvarTypical
- rs4783244G;GNormalTypical
- rs6565105G;Gcommon in clinvarTypical
- rs9939760G;Gcommon genotypeTypical
- rs11646411C;Ccommon in complete genomicsTypical
- rs12051272G;Gcommon in complete genomicsTypical
- rs12386026C;Ccommon in complete genomicsTypical
- rs17216786C;Ccommon in complete genomicsTypical
Notes
From SNPedia
Notes
rs8055236 has been reported in a large study to be associated with heart disease, in particular, coronary artery disease. The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.91 (CI 1.33-2.74), and for homozygotes, 2.23 (CI 1.56-3.17).
Source and license
Adapted from rs8055236 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.