rs11212617
A SNP in the C11orf65 gene on chromosome 11. Its most notable genotype is A;C: Somewhat increased likelihood of treatment success with metformin
- Gene
- C11orf65
- Location
- Chr 11108,412,434 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 47%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodnormal response to Metformin
- A;CMost notableGoodSomewhat increased likelihood of treatment success with metformin
- C;CGoodSomewhat increased likelihood of treatment success with metformin
On SNPedia: (A;A), (A;C), (C;C). 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 22% A;C 39% C;C 39%
- European ancestry (Utah)A;A 27% A;C 54% C;C 20%
- Han Chinese (Beijing)A;A 16% A;C 39% C;C 45%
- Japanese (Tokyo)A;A 20% A;C 41% C;C 40%
- Yoruba (Nigeria)A;A 2% A;C 32% C;C 66%
- African ancestry (Southwest US)A;A 18% A;C 37% C;C 46%
- Chinese (Denver)A;A 17% A;C 50% C;C 34%
- Gujarati IndianA;A 47% A;C 39% C;C 15%
- Luhya (Kenya)A;A 4% A;C 30% C;C 67%
- Mexican ancestry (Los Angeles)A;A 36% A;C 41% C;C 22%
- Maasai (Kenya)A;A 8% A;C 33% C;C 59%
- TuscanA;A 54% A;C 33% C;C 13%
Related
Conditions, medicines and genes
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
Notes
From SNPedia
Notes
Influences Metformin response
Source and license
Adapted from rs11212617 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.