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rs397507792

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507792(-;-)
Make rs397507792(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339979
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507792
ClinGenrs397507792
ebirs397507792
HLIrs397507792
Exacrs397507792
Varsomers397507792
Maprs397507792
PheGenIrs397507792
hapmaprs397507792
1000 genomesrs397507792
hgdprs397507792
ensemblrs397507792
gopubmedrs397507792
geneviewrs397507792
scholarrs397507792
googlers397507792
pharmgkbrs397507792
gwascentralrs397507792
openSNPrs397507792
23andMers397507792
23andMe allrs397507792
SNP Nexus

SNPshotrs397507792
SNPdbers397507792
MSV3drs397507792
GWAS Ctlgrs397507792
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397507792(A;A)
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.32914116delA
CLNSRC ClinVar
CLNACC RCV000044699.2, RCV000257129.2,