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rs397508006

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508006(A;A)
Make rs397508006(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376792
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508006
ebirs397508006
HLIrs397508006
Exacrs397508006
Varsomers397508006
Maprs397508006
PheGenIrs397508006
hapmaprs397508006
1000 genomesrs397508006
hgdprs397508006
ensemblrs397508006
gopubmedrs397508006
geneviewrs397508006
scholarrs397508006
googlers397508006
pharmgkbrs397508006
gwascentralrs397508006
openSNPrs397508006
23andMers397508006
23andMe allrs397508006
SNP Nexus

SNPshotrs397508006
SNPdbers397508006
MSV3drs397508006
GWAS Ctlgrs397508006
Max Magnitude0
ClinVar
Risk rs397508006(A;A)
Alt rs397508006(A;A)
Reference rs397508006(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32950929G>A
CLNSRC ClinVar
CLNACC RCV000045613.2, RCV000239149.1,