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rs397507422

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507422(-;-)
Make rs397507422(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32380124
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507422
ebirs397507422
HLIrs397507422
Exacrs397507422
Varsomers397507422
Maprs397507422
PheGenIrs397507422
hapmaprs397507422
1000 genomesrs397507422
hgdprs397507422
ensemblrs397507422
gopubmedrs397507422
geneviewrs397507422
scholarrs397507422
googlers397507422
pharmgkbrs397507422
gwascentralrs397507422
openSNPrs397507422
23andMers397507422
23andMe allrs397507422
SNP Nexus

SNPshotrs397507422
SNPdbers397507422
MSV3drs397507422
GWAS Ctlgrs397507422
Max Magnitude0
ClinVar
Risk rs397507422(;)
Alt rs397507422(;)
Reference rs397507422(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32954261delG
CLNSRC ClinVar
CLNACC RCV000031804.3, RCV000235872.1,