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rs397507591

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507591(-;-)
Make rs397507591(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332977
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507591
ebirs397507591
HLIrs397507591
Exacrs397507591
Varsomers397507591
Maprs397507591
PheGenIrs397507591
hapmaprs397507591
1000 genomesrs397507591
hgdprs397507591
ensemblrs397507591
gopubmedrs397507591
geneviewrs397507591
scholarrs397507591
googlers397507591
pharmgkbrs397507591
gwascentralrs397507591
openSNPrs397507591
23andMers397507591
23andMe allrs397507591
SNP Nexus

SNPshotrs397507591
SNPdbers397507591
MSV3drs397507591
GWAS Ctlgrs397507591
Max Magnitude0
ClinVar
Risk rs397507591(;)
Alt rs397507591(;)
Reference rs397507591(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907114delG
CLNSRC ClinVar
CLNACC RCV000043818.2, RCV000077258.2,