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rs397507645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507645(-;-)
Make rs397507645(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337225
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507645
ebirs397507645
HLIrs397507645
Exacrs397507645
Varsomers397507645
Maprs397507645
PheGenIrs397507645
hapmaprs397507645
1000 genomesrs397507645
hgdprs397507645
ensemblrs397507645
gopubmedrs397507645
geneviewrs397507645
scholarrs397507645
googlers397507645
pharmgkbrs397507645
gwascentralrs397507645
openSNPrs397507645
23andMers397507645
23andMe allrs397507645
SNP Nexus

SNPshotrs397507645
SNPdbers397507645
MSV3drs397507645
GWAS Ctlgrs397507645
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397507645(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.32911362delA
CLNSRC ClinVar
CLNACC RCV000044078.2, RCV000257652.2,