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rs397508025

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508025(A;A)
Make rs397508025(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379774
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508025
ebirs397508025
HLIrs397508025
Exacrs397508025
Varsomers397508025
Maprs397508025
PheGenIrs397508025
hapmaprs397508025
1000 genomesrs397508025
hgdprs397508025
ensemblrs397508025
gopubmedrs397508025
geneviewrs397508025
scholarrs397508025
googlers397508025
pharmgkbrs397508025
gwascentralrs397508025
openSNPrs397508025
23andMers397508025
23andMe allrs397508025
SNP Nexus

SNPshotrs397508025
SNPdbers397508025
MSV3drs397508025
GWAS Ctlgrs397508025
Max Magnitude0
ClinVar
Risk rs397508025(A,G;A,G)
Alt rs397508025(A,G;A,G)
Reference rs397508025(C;C)
Significance Pathogenic
Disease Familial cancer of breast not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32953911C>A; NC_000013.10:g.32953911C>G
CLNSRC ClinVar
CLNACC RCV000045677.2, RCV000160161.2, RCV000221983.1,