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rs13294895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
(C;T) 1.4 slightly increased risk for breast cancer (1.09x)
(T;T) 1.4 slightly increased risk for breast cancer (1.18x)
ReferenceGRCh38 38.1/142
Chromosome9
Position108074895
is asnp
is mentioned by
dbSNPrs13294895
ebirs13294895
HLIrs13294895
Exacrs13294895
Varsomers13294895
Maprs13294895
PheGenIrs13294895
hapmaprs13294895
1000 genomesrs13294895
hgdprs13294895
ensemblrs13294895
gopubmedrs13294895
geneviewrs13294895
scholarrs13294895
googlers13294895
pharmgkbrs13294895
gwascentralrs13294895
openSNPrs13294895
23andMers13294895
23andMe allrs13294895
SNP Nexus

SNPshotrs13294895
SNPdbers13294895
MSV3drs13294895
GWAS Ctlgrs13294895
Max Magnitude1.4

rs13294895 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 rs13294895(T) allele was independently associated with increased risk in Europeans (odds ratio 1.09, CI:1.06-1.12, p = 2.97 × 10e-11) but not in Asians.[PMID 25652398OA-icon.png]

? (C;C) (C;T) (T;T) 28
[PMID 25652398OA-icon.png] Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2