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rs397507430

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507430(G;T)
Make rs397507430(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32396919
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507430
ebirs397507430
HLIrs397507430
Exacrs397507430
Varsomers397507430
Maprs397507430
PheGenIrs397507430
hapmaprs397507430
1000 genomesrs397507430
hgdprs397507430
ensemblrs397507430
gopubmedrs397507430
geneviewrs397507430
scholarrs397507430
googlers397507430
pharmgkbrs397507430
gwascentralrs397507430
openSNPrs397507430
23andMers397507430
23andMe allrs397507430
SNP Nexus

SNPshotrs397507430
SNPdbers397507430
MSV3drs397507430
GWAS Ctlgrs397507430
Max Magnitude0
ClinVar
Risk rs397507430(T;T)
Alt rs397507430(T;T)
Reference rs397507430(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32971056G>T
CLNSRC ClinVar
CLNACC RCV000031829.3,