rs786203631
A SNP in the C11orf65 gene on chromosome 11. Its most notable genotype is C;G: Breast cancer associated mutation
- Gene
- C11orf65
- Location
- Chr 11108,365,219 (GRCh38)
- Highest magnitude
- 6.0Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;GMost notableBadBreast cancer associated mutation
- G;GGoodcommon in clinvar
On SNPedia: (C;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
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 rs786203631 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.