rs11213809
A SNP in the C11orf53 gene on chromosome 11. Its most notable genotype is G;G: common/normal
- Gene
- C11orf53
- Location
- Chr 11111,265,020 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
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 10 HapMap populations.
- AverageG;G 62%
- European ancestry (Utah)G;G 50%
- Han Chinese (Beijing)G;G 71%
- Japanese (Tokyo)G;G 78%
- Yoruba (Nigeria)G;G 68%
- Chinese (Denver)G;G 56%
- Gujarati IndianG;G 60%
- Luhya (Kenya)G;G 69%
- Mexican ancestry (Los Angeles)G;G 71%
- Maasai (Kenya)G;G 53%
- TuscanG;G 50%
Notes
From SNPedia
Notes
Strongly enhanced colorectal cancer risk stratification by combining family history and genetic risk score
Source and license
Adapted from rs11213809 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.