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rs397509096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509096(-;-)
Make rs397509096(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091816
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509096
ebirs397509096
HLIrs397509096
Exacrs397509096
Varsomers397509096
Maprs397509096
PheGenIrs397509096
hapmaprs397509096
1000 genomesrs397509096
hgdprs397509096
ensemblrs397509096
gopubmedrs397509096
geneviewrs397509096
scholarrs397509096
googlers397509096
pharmgkbrs397509096
gwascentralrs397509096
openSNPrs397509096
23andMers397509096
23andMe allrs397509096
SNP Nexus

SNPshotrs397509096
SNPdbers397509096
MSV3drs397509096
GWAS Ctlgrs397509096
Max Magnitude0
ClinVar
Risk rs397509096(;)
Alt rs397509096(;)
Reference rs397509096(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.41243833delA
CLNSRC ClinVar
CLNACC RCV000048299.2,