rs4783244
A SNP in the CDH13 gene on chromosome 16. Its most notable genotype is G;G: Normal
- Gene
- CDH13
- Location
- Chr 1682,628,663 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 34%
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GMost notableNot ratedNormal
- G;TNot ratedAdiponectin levels significantly decreased x0.34 SD
- T;TNot ratedAdiponectin levels significantly decreased x0.68 SD
On SNPedia: (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.
- AverageG;G 47% G;T 43% T;T 10%
- European ancestry (Utah)G;G 30% G;T 52% T;T 18%
- Han Chinese (Beijing)G;G 48% G;T 44% T;T 8%
- Japanese (Tokyo)G;G 45% G;T 44% T;T 11%
- Yoruba (Nigeria)G;G 61% G;T 36% T;T 3%
- African ancestry (Southwest US)G;G 54% G;T 42% T;T 4%
- Chinese (Denver)G;G 52% G;T 39% T;T 8%
- Gujarati IndianG;G 32% G;T 51% T;T 18%
- Luhya (Kenya)G;G 52% G;T 42% T;T 6%
- Mexican ancestry (Los Angeles)G;G 57% G;T 33% T;T 10%
- Maasai (Kenya)G;G 45% G;T 46% T;T 9%
- TuscanG;G 39% G;T 44% T;T 17%
Related
Other CDH13 SNPs
- rs8055236G;Gcommon, but 2.2x higher risk for heart diseaseMinor
- rs1048612A;Acommon in clinvarTypical
- 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
Source and license
Adapted from rs4783244 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.