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rs397509151

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509151(C;T)
Make rs397509151(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082560
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509151
ebirs397509151
HLIrs397509151
Exacrs397509151
Varsomers397509151
Maprs397509151
PheGenIrs397509151
hapmaprs397509151
1000 genomesrs397509151
hgdprs397509151
ensemblrs397509151
gopubmedrs397509151
geneviewrs397509151
scholarrs397509151
googlers397509151
pharmgkbrs397509151
gwascentralrs397509151
openSNPrs397509151
23andMers397509151
23andMe allrs397509151
SNP Nexus

SNPshotrs397509151
SNPdbers397509151
MSV3drs397509151
GWAS Ctlgrs397509151
Max Magnitude0
ClinVar
Risk rs397509151(T;T)
Alt rs397509151(T;T)
Reference rs397509151(C;C)
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.41234577G>A
CLNSRC ClinVar
CLNACC RCV000048485.2, RCV000077567.2,