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rs397507404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507404(A;A)
Make rs397507404(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370955
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507404
ebirs397507404
HLIrs397507404
Exacrs397507404
Varsomers397507404
Maprs397507404
PheGenIrs397507404
hapmaprs397507404
1000 genomesrs397507404
hgdprs397507404
ensemblrs397507404
gopubmedrs397507404
geneviewrs397507404
scholarrs397507404
googlers397507404
pharmgkbrs397507404
gwascentralrs397507404
openSNPrs397507404
23andMers397507404
23andMe allrs397507404
SNP Nexus

SNPshotrs397507404
SNPdbers397507404
MSV3drs397507404
GWAS Ctlgrs397507404
Max Magnitude0
ClinVar
Risk rs397507404(A;A)
Alt rs397507404(A;A)
Reference rs397507404(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer not provided Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32945092G>A
CLNSRC ClinVar
CLNACC RCV000031747.3, RCV000160152.2, RCV000213906.1, RCV000231355.1,