rs9939760
A SNP in the CDH13 gene on chromosome 16. Its most notable genotype is G;G: common genotype
- Gene
- CDH13
- Location
- Chr 1683,619,297 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageG;G 67%
- European ancestry (Utah)G;G 99%
- Han Chinese (Beijing)G;G 55%
- Japanese (Tokyo)G;G 51%
- Yoruba (Nigeria)G;G 50%
- African ancestry (Southwest US)G;G 58%
- Chinese (Denver)G;G 50%
- Gujarati IndianG;G 90%
- Luhya (Kenya)G;G 50%
- Mexican ancestry (Los Angeles)G;G 81%
- Maasai (Kenya)G;G 53%
- TuscanG;G 98%
Related
Other CDH13 SNPs
- rs8055236G;Gcommon, but 2.2x higher risk for heart diseaseMinor
- rs1048612A;Acommon in clinvarTypical
- rs4783244G;GNormalTypical
- rs6565105G;Gcommon in clinvarTypical
- rs11646411C;Ccommon in complete genomicsTypical
- rs12051272G;Gcommon in complete genomicsTypical
- rs12386026C;Ccommon in complete genomicsTypical
- rs17216786C;Ccommon in complete genomicsTypical
Source and license
Adapted from rs9939760 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.