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rs397509111

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509111(-;-)
Make rs397509111(-;T)
Make rs397509111(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091708
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509111
ebirs397509111
HLIrs397509111
Exacrs397509111
Varsomers397509111
Maprs397509111
PheGenIrs397509111
hapmaprs397509111
1000 genomesrs397509111
hgdprs397509111
ensemblrs397509111
gopubmedrs397509111
geneviewrs397509111
scholarrs397509111
googlers397509111
pharmgkbrs397509111
gwascentralrs397509111
openSNPrs397509111
23andMers397509111
23andMe allrs397509111
SNP Nexus

SNPshotrs397509111
SNPdbers397509111
MSV3drs397509111
GWAS Ctlgrs397509111
Max Magnitude0
ClinVar
Risk rs397509111(T;T)
Alt rs397509111(T;T)
Reference rs397509111(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243725_41243726insA
CLNSRC ClinVar
CLNACC RCV000048345.2,