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rs397509091

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509091(G;G)
Make rs397509091(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091884
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509091
ebirs397509091
HLIrs397509091
Exacrs397509091
Varsomers397509091
Maprs397509091
PheGenIrs397509091
hapmaprs397509091
1000 genomesrs397509091
hgdprs397509091
ensemblrs397509091
gopubmedrs397509091
geneviewrs397509091
scholarrs397509091
googlers397509091
pharmgkbrs397509091
gwascentralrs397509091
openSNPrs397509091
23andMers397509091
23andMe allrs397509091
SNP Nexus

SNPshotrs397509091
SNPdbers397509091
MSV3drs397509091
GWAS Ctlgrs397509091
Max Magnitude0
ClinVar
Risk rs397509091(G;G)
Alt rs397509091(G;G)
Reference rs397509091(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243901A>C
CLNSRC ClinVar
CLNACC RCV000048269.2,