rs659243
A SNP in the C11orf65 gene on chromosome 11. Its most notable genotype is A;A: common in clinvar
- Gene
- C11orf65
- Location
- Chr 11108,312,440 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 0%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageA;A 0% G;G 98%
- European ancestry (Utah)A;A 0% G;G 99%
- Han Chinese (Beijing)A;A 0% G;G 99%
- Japanese (Tokyo)A;A 0% G;G 97%
- Yoruba (Nigeria)A;A 0% G;G 99%
- Chinese (Denver)A;A 0% G;G 99%
- Gujarati IndianA;A 0% G;G 99%
- Luhya (Kenya)A;A 0% G;G 98%
- Mexican ancestry (Los Angeles)A;A 0% G;G 95%
- TuscanA;A 0% G;G 99%
Related
Other C11orf65 SNPs
- rs28904921G;T~8 fold increase in relative risk for breast cancerVery important
- rs17174393C;GBreast cancer associated mutationVery important
- rs564652222C;TBreast cancer associated mutationVery important
- rs587779852G;TBreast cancer associated mutationVery important
- rs587779861C;TBreast cancer associated mutationVery important
- rs587779866A;CBreast cancer associated mutationVery important
- rs587781302A;GBreast cancer associated mutationVery important
- rs587781584A;GBreast cancer associated mutationVery important
Source and license
Adapted from rs659243 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.