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rs397507981

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507981(A;A)
Make rs397507981(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370434
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507981
ebirs397507981
HLIrs397507981
Exacrs397507981
Varsomers397507981
Maprs397507981
PheGenIrs397507981
hapmaprs397507981
1000 genomesrs397507981
hgdprs397507981
ensemblrs397507981
gopubmedrs397507981
geneviewrs397507981
scholarrs397507981
googlers397507981
pharmgkbrs397507981
gwascentralrs397507981
openSNPrs397507981
23andMers397507981
23andMe allrs397507981
SNP Nexus

SNPshotrs397507981
SNPdbers397507981
MSV3drs397507981
GWAS Ctlgrs397507981
Max Magnitude0
ClinVar
Risk rs397507981(A;A)
Alt rs397507981(A;A)
Reference rs397507981(G;G)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000013.10:g.32944571G>A
CLNSRC ClinVar
CLNACC RCV000045496.2, RCV000216791.1, RCV000236926.1,