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rs397509079

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509079(G;T)
Make rs397509079(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092017
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509079
ebirs397509079
HLIrs397509079
Exacrs397509079
Varsomers397509079
Maprs397509079
PheGenIrs397509079
hapmaprs397509079
1000 genomesrs397509079
hgdprs397509079
ensemblrs397509079
gopubmedrs397509079
geneviewrs397509079
scholarrs397509079
googlers397509079
pharmgkbrs397509079
gwascentralrs397509079
openSNPrs397509079
23andMers397509079
23andMe allrs397509079
SNP Nexus

SNPshotrs397509079
SNPdbers397509079
MSV3drs397509079
GWAS Ctlgrs397509079
Max Magnitude0
ClinVar
Risk rs397509079(T;T)
Alt rs397509079(T;T)
Reference rs397509079(G;G)
Significance Pathogenic
Disease Familial cancer of breast not provided
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast not provided
Reversed 1
HGVS NC_000017.10:g.41244034C>A
CLNSRC ClinVar
CLNACC RCV000048221.2, RCV000236268.1,