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rs397507943

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507943(-;-)
Make rs397507943(-;A)
Make rs397507943(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362601
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507943
ebirs397507943
HLIrs397507943
Exacrs397507943
Varsomers397507943
Maprs397507943
PheGenIrs397507943
hapmaprs397507943
1000 genomesrs397507943
hgdprs397507943
ensemblrs397507943
gopubmedrs397507943
geneviewrs397507943
scholarrs397507943
googlers397507943
pharmgkbrs397507943
gwascentralrs397507943
openSNPrs397507943
23andMers397507943
23andMe allrs397507943
SNP Nexus

SNPshotrs397507943
SNPdbers397507943
MSV3drs397507943
GWAS Ctlgrs397507943
Max Magnitude0
ClinVar
Risk rs397507943(A;A)
Alt rs397507943(A;A)
Reference rs397507943(;)
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.32936738dupA
CLNSRC ClinVar
CLNACC RCV000045338.2, RCV000225658.1,