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rs397509141

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397509141(-;-)
Make rs397509141(-;CT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43090992
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509141
ebirs397509141
HLIrs397509141
Exacrs397509141
Varsomers397509141
Maprs397509141
PheGenIrs397509141
hapmaprs397509141
1000 genomesrs397509141
hgdprs397509141
ensemblrs397509141
gopubmedrs397509141
geneviewrs397509141
scholarrs397509141
googlers397509141
pharmgkbrs397509141
gwascentralrs397509141
openSNPrs397509141
23andMers397509141
23andMe allrs397509141
SNP Nexus

SNPshotrs397509141
SNPdbers397509141
MSV3drs397509141
GWAS Ctlgrs397509141
Max Magnitude0
ClinVar
Risk rs397509141(;)
Alt rs397509141(;)
Reference rs397509141(CT;CT)
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.41243009_41243010delAG
CLNSRC ClinVar
CLNACC RCV000048457.2, RCV000239228.1,