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rs397509115

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509115(-;-)
Make rs397509115(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091655
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509115
ebirs397509115
HLIrs397509115
Exacrs397509115
Varsomers397509115
Maprs397509115
PheGenIrs397509115
hapmaprs397509115
1000 genomesrs397509115
hgdprs397509115
ensemblrs397509115
gopubmedrs397509115
geneviewrs397509115
scholarrs397509115
googlers397509115
pharmgkbrs397509115
gwascentralrs397509115
openSNPrs397509115
23andMers397509115
23andMe allrs397509115
SNP Nexus

SNPshotrs397509115
SNPdbers397509115
MSV3drs397509115
GWAS Ctlgrs397509115
Max Magnitude0
ClinVar
Risk rs397509115(;)
Alt rs397509115(;)
Reference rs397509115(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.41243672delA
CLNSRC ClinVar
CLNACC RCV000048364.2,