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rs397508908

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;A) 6 BRCA1 variant considered pathogenic for breast cancer
(A;A) 0 common in clinvar


Make rs397508908(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093726
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508908
dbSNP (old)rs397508908
ClinGenrs397508908
ebirs397508908
HLIrs397508908
Exacrs397508908
Gnomadrs397508908
Varsomers397508908
Maprs397508908
PheGenIrs397508908
Biobankrs397508908
1000 genomesrs397508908
hgdprs397508908
ensemblrs397508908
gopubmedrs397508908
geneviewrs397508908
scholarrs397508908
googlers397508908
pharmgkbrs397508908
gwascentralrs397508908
openSNPrs397508908
23andMers397508908
23andMe allrs397508908
SNP Nexus

SNPshotrs397508908
SNPdbers397508908
MSV3drs397508908
GWAS Ctlgrs397508908
Max Magnitude6
ClinVar
Risk rs397508908(-;-)
Alt rs397508908(-;-)
Reference Rs397508908(A;A)
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.41245743delT
CLNSRC ClinVar
CLNACC RCV000047591.2, RCV000257371.2,