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rs397509074

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509074(-;-)
Make rs397509074(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092050
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509074
ClinGenrs397509074
ebirs397509074
HLIrs397509074
Exacrs397509074
Varsomers397509074
Maprs397509074
PheGenIrs397509074
hapmaprs397509074
1000 genomesrs397509074
hgdprs397509074
ensemblrs397509074
gopubmedrs397509074
geneviewrs397509074
scholarrs397509074
googlers397509074
pharmgkbrs397509074
gwascentralrs397509074
openSNPrs397509074
23andMers397509074
23andMe allrs397509074
SNP Nexus

SNPshotrs397509074
SNPdbers397509074
MSV3drs397509074
GWAS Ctlgrs397509074
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397509074(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.41244067delC
CLNSRC ClinVar
CLNACC RCV000048212.2,