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rs397507279

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507279(A;A)
Make rs397507279(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336325
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507279
ebirs397507279
HLIrs397507279
Exacrs397507279
Varsomers397507279
Maprs397507279
PheGenIrs397507279
hapmaprs397507279
1000 genomesrs397507279
hgdprs397507279
ensemblrs397507279
gopubmedrs397507279
geneviewrs397507279
scholarrs397507279
googlers397507279
pharmgkbrs397507279
gwascentralrs397507279
openSNPrs397507279
23andMers397507279
23andMe allrs397507279
SNP Nexus

SNPshotrs397507279
SNPdbers397507279
MSV3drs397507279
GWAS Ctlgrs397507279
Max Magnitude0
ClinVar
Risk rs397507279(A;A)
Alt rs397507279(A;A)
Reference rs397507279(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32910462T>A
CLNSRC ClinVar
CLNACC RCV000031352.3, RCV000223168.1,