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rs397508903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508903(G;T)
Make rs397508903(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093802
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508903
ebirs397508903
HLIrs397508903
Exacrs397508903
Varsomers397508903
Maprs397508903
PheGenIrs397508903
hapmaprs397508903
1000 genomesrs397508903
hgdprs397508903
ensemblrs397508903
gopubmedrs397508903
geneviewrs397508903
scholarrs397508903
googlers397508903
pharmgkbrs397508903
gwascentralrs397508903
openSNPrs397508903
23andMers397508903
23andMe allrs397508903
SNP Nexus

SNPshotrs397508903
SNPdbers397508903
MSV3drs397508903
GWAS Ctlgrs397508903
Max Magnitude0
ClinVar
Risk rs397508903(C;C) rs397508903(T;T)
Alt rs397508903(C;C) rs397508903(T;T)
Reference Rs397508903(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41245819C>A
CLNSRC ClinVar
CLNACC RCV000047570.2, RCV000257813.2,