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rs10816625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common/normal
(A;G) 1.5 slightly increased risk for breast cancer (1.12x)
(G;G) 1.5 slightly increased risk for breast cancer (1.24x)
ReferenceGRCh38 38.1/142
Chromosome9
Position108074792
is asnp
is mentioned by
dbSNPrs10816625
ebirs10816625
HLIrs10816625
Exacrs10816625
Varsomers10816625
Maprs10816625
PheGenIrs10816625
hapmaprs10816625
1000 genomesrs10816625
hgdprs10816625
ensemblrs10816625
gopubmedrs10816625
geneviewrs10816625
scholarrs10816625
googlers10816625
pharmgkbrs10816625
gwascentralrs10816625
openSNPrs10816625
23andMers10816625
23andMe allrs10816625
SNP Nexus

SNPshotrs10816625
SNPdbers10816625
MSV3drs10816625
GWAS Ctlgrs10816625
Max Magnitude1.5

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).[PMID 25652398OA-icon.png]

? (A;A) (A;G) (G;G) 28