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rs397507930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507930(-;-)
Make rs397507930(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32331004
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507930
ebirs397507930
HLIrs397507930
Exacrs397507930
Varsomers397507930
Maprs397507930
PheGenIrs397507930
hapmaprs397507930
1000 genomesrs397507930
hgdprs397507930
ensemblrs397507930
gopubmedrs397507930
geneviewrs397507930
scholarrs397507930
googlers397507930
pharmgkbrs397507930
gwascentralrs397507930
openSNPrs397507930
23andMers397507930
23andMe allrs397507930
SNP Nexus

SNPshotrs397507930
SNPdbers397507930
MSV3drs397507930
GWAS Ctlgrs397507930
Max Magnitude0
ClinVar
Risk rs397507930(;)
Alt rs397507930(;)
Reference rs397507930(C;C)
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.32905141delC
CLNSRC ClinVar
CLNACC RCV000045283.2, RCV000225568.1,