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rs397507663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507663(C;G)
Make rs397507663(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337651
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507663
ebirs397507663
HLIrs397507663
Exacrs397507663
Varsomers397507663
Maprs397507663
PheGenIrs397507663
hapmaprs397507663
1000 genomesrs397507663
hgdprs397507663
ensemblrs397507663
gopubmedrs397507663
geneviewrs397507663
scholarrs397507663
googlers397507663
pharmgkbrs397507663
gwascentralrs397507663
openSNPrs397507663
23andMers397507663
23andMe allrs397507663
SNP Nexus

SNPshotrs397507663
SNPdbers397507663
MSV3drs397507663
GWAS Ctlgrs397507663
Max Magnitude0
ClinVar
Risk rs397507663(A,G;A,G)
Alt rs397507663(A,G;A,G)
Reference rs397507663(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911788C>A; NC_000013.10:g.32911788C>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000131361.2, RCV000044172.2,