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rs397509113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509113(-;-)
Make rs397509113(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091687
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509113
ebirs397509113
HLIrs397509113
Exacrs397509113
Varsomers397509113
Maprs397509113
PheGenIrs397509113
hapmaprs397509113
1000 genomesrs397509113
hgdprs397509113
ensemblrs397509113
gopubmedrs397509113
geneviewrs397509113
scholarrs397509113
googlers397509113
pharmgkbrs397509113
gwascentralrs397509113
openSNPrs397509113
23andMers397509113
23andMe allrs397509113
SNP Nexus

SNPshotrs397509113
SNPdbers397509113
MSV3drs397509113
GWAS Ctlgrs397509113
Max Magnitude0
ClinVar
Risk rs397509113(;)
Alt rs397509113(;)
Reference rs397509113(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243704delC
CLNSRC ClinVar
CLNACC RCV000048354.2,