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rs397507346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507346(C;G)
Make rs397507346(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339355
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507346
ebirs397507346
HLIrs397507346
Exacrs397507346
Varsomers397507346
Maprs397507346
PheGenIrs397507346
hapmaprs397507346
1000 genomesrs397507346
hgdprs397507346
ensemblrs397507346
gopubmedrs397507346
geneviewrs397507346
scholarrs397507346
googlers397507346
pharmgkbrs397507346
gwascentralrs397507346
openSNPrs397507346
23andMers397507346
23andMe allrs397507346
SNP Nexus

SNPshotrs397507346
SNPdbers397507346
MSV3drs397507346
GWAS Ctlgrs397507346
Max Magnitude0
ClinVar
Risk rs397507346(G;G)
Alt rs397507346(G;G)
Reference rs397507346(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913492C>G
CLNSRC ClinVar
CLNACC RCV000031519.3,