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rs397507797

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507797(A;A)
Make rs397507797(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340054
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507797
ebirs397507797
HLIrs397507797
Exacrs397507797
Varsomers397507797
Maprs397507797
PheGenIrs397507797
hapmaprs397507797
1000 genomesrs397507797
hgdprs397507797
ensemblrs397507797
gopubmedrs397507797
geneviewrs397507797
scholarrs397507797
googlers397507797
pharmgkbrs397507797
gwascentralrs397507797
openSNPrs397507797
23andMers397507797
23andMe allrs397507797
SNP Nexus

SNPshotrs397507797
SNPdbers397507797
MSV3drs397507797
GWAS Ctlgrs397507797
Max Magnitude0
ClinVar
Risk rs397507797(A;A)
Alt rs397507797(A;A)
Reference rs397507797(C;C)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32914191C>A; NC_000013.10:g.32914191C>G
CLNSRC ClinVar
CLNACC RCV000044721.2, RCV000215854.1,