Rs11571747

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Orientationplus
Geno Mag Summary
(A;A) 0 common in complete genomics
(C;C) 2
Make rs11571747(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371035
GeneBRCA2
is asnp
is mentioned by
dbSNPrs11571747
Exacrs11571747
PheGenIrs11571747
nextbiors11571747
hapmaprs11571747
1000 genomesrs11571747
hgdprs11571747
ensemblrs11571747
gopubmedrs11571747
geneviewrs11571747
scholarrs11571747
googlers11571747
pharmgkbrs11571747
gwascentralrs11571747
openSNPrs11571747
23andMers11571747
23andMe allrs11571747
SNP Nexus

SNPshotrs11571747
SNPdbers11571747
MSV3drs11571747
GMAF0.0004591
Max Magnitude2
? (A;A) (A;C) (C;C) 28

This SNP, a variant in the BRCA2 gene, is 1 of 25 SNPs reported to represent independently minor, but cumulatively significant, increased risk for breast cancer. [PMID 17341484]

For details of all 25 SNPs in this group, along with the two methods used to calculate overall risk estimates for breast cancer, refer to the SNPedia breast cancer entry.

For this particular SNP, the risk (minor) allele is (C).

Neighborrs11571746
Distance64


ClinVar
Risk rs11571747(C;C)
Alt rs11571747(C;C)
Reference rs11571747(A;A)
Significance Probable-non-pathogenic
Disease Breast-ovarian cancer not provided Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32945172A>C
CLNSRC
CLNACC RCV000031751.3, RCV000034464.1, RCV000045558.2,