rs10816625
A SNP in the LOC105376214 gene on chromosome 9. Its most notable genotype is A;G: slightly increased risk for breast cancer (1.12x)
- Gene
- LOC105376214
- Location
- Chr 9108,074,792 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodcommon/normal
- A;GMost notableBadslightly increased risk for breast cancer (1.12x)
- G;GBadslightly increased risk for breast cancer (1.24x)
On SNPedia: (A;A), (A;G), (G;G). 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 72% A;G 22% G;G 7%
- European ancestry (Utah)A;A 84% A;G 13% G;G 3%
- Han Chinese (Beijing)A;A 24% A;G 52% G;G 24%
- Japanese (Tokyo)A;A 37% A;G 50% G;G 12%
- Yoruba (Nigeria)A;A 100% A;G 0% G;G 0%
- African ancestry (Southwest US)A;A 95% A;G 5% G;G 0%
- Chinese (Denver)A;A 31% A;G 51% G;G 18%
- Gujarati IndianA;A 81% A;G 18% G;G 1%
- Luhya (Kenya)A;A 98% A;G 2% G;G 0%
- Mexican ancestry (Los Angeles)A;A 57% A;G 31% G;G 12%
- Maasai (Kenya)A;A 99% A;G <1% G;G 0%
- TuscanA;A 83% A;G 16% G;G 1%
Related
Conditions, medicines and genes
Other LOC105376214 SNPs
Notes
From SNPedia
Notes
rs10816625 is a SNP in a region of chromosome 9q31.2 that has been associated with breast cancer. In a pooled study of 52 studies totalling 43,160 breast cancer cases in women of European ancestry, plus a further 5795 cases of Asian ancestry, the rs10816625(G) allele was independently associated with increased risk in both Europeans (odds ratio 1.12, CI:1.08-1.17, p = 7.89 × 10e-9) and Asians (odds ratio 1.12, CI:1.06-1.18, p = 2.77 × 10e-5).
A;G
see discussion at rs10816625
G;G
see discussion at rs10816625
Source and license
Adapted from rs10816625 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.