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rs397507276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507276(A;G)
Make rs397507276(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333277
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507276
ebirs397507276
HLIrs397507276
Exacrs397507276
Varsomers397507276
Maprs397507276
PheGenIrs397507276
hapmaprs397507276
1000 genomesrs397507276
hgdprs397507276
ensemblrs397507276
gopubmedrs397507276
geneviewrs397507276
scholarrs397507276
googlers397507276
pharmgkbrs397507276
gwascentralrs397507276
openSNPrs397507276
23andMers397507276
23andMe allrs397507276
SNP Nexus

SNPshotrs397507276
SNPdbers397507276
MSV3drs397507276
GWAS Ctlgrs397507276
Max Magnitude0
ClinVar
Risk rs397507276(G;G)
Alt rs397507276(G;G)
Reference rs397507276(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907414A>G
CLNSRC ClinVar
CLNACC RCV000031338.3,