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rs397507646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507646(G;T)
Make rs397507646(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319298
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507646
ebirs397507646
HLIrs397507646
Exacrs397507646
Varsomers397507646
Maprs397507646
PheGenIrs397507646
hapmaprs397507646
1000 genomesrs397507646
hgdprs397507646
ensemblrs397507646
gopubmedrs397507646
geneviewrs397507646
scholarrs397507646
googlers397507646
pharmgkbrs397507646
gwascentralrs397507646
openSNPrs397507646
23andMers397507646
23andMe allrs397507646
SNP Nexus

SNPshotrs397507646
SNPdbers397507646
MSV3drs397507646
GWAS Ctlgrs397507646
Max Magnitude0
ClinVar
Risk rs397507646(T;T)
Alt rs397507646(T;T)
Reference rs397507646(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32893435G>T
CLNSRC ClinVar
CLNACC RCV000044083.2, RCV000083095.2, RCV000166898.1, RCV000214710.1,