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rs397507278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507278(A;A)
Make rs397507278(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333328
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507278
ebirs397507278
HLIrs397507278
Exacrs397507278
Varsomers397507278
Maprs397507278
PheGenIrs397507278
hapmaprs397507278
1000 genomesrs397507278
hgdprs397507278
ensemblrs397507278
gopubmedrs397507278
geneviewrs397507278
scholarrs397507278
googlers397507278
pharmgkbrs397507278
gwascentralrs397507278
openSNPrs397507278
23andMers397507278
23andMe allrs397507278
SNP Nexus

SNPshotrs397507278
SNPdbers397507278
MSV3drs397507278
GWAS Ctlgrs397507278
Max Magnitude0
ClinVar
Risk rs397507278(A,G;A,G)
Alt rs397507278(A,G;A,G)
Reference rs397507278(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.32907465C>A; NC_000013.10:g.32907465C>G
CLNSRC ClinVar
CLNACC RCV000031346.3, RCV000031347.3,