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rs397509042

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509042(-;-)
Make rs397509042(-;G)
Make rs397509042(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092373
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509042
ebirs397509042
HLIrs397509042
Exacrs397509042
Varsomers397509042
Maprs397509042
PheGenIrs397509042
hapmaprs397509042
1000 genomesrs397509042
hgdprs397509042
ensemblrs397509042
gopubmedrs397509042
geneviewrs397509042
scholarrs397509042
googlers397509042
pharmgkbrs397509042
gwascentralrs397509042
openSNPrs397509042
23andMers397509042
23andMe allrs397509042
SNP Nexus

SNPshotrs397509042
SNPdbers397509042
MSV3drs397509042
GWAS Ctlgrs397509042
Max Magnitude0
ClinVar
Risk rs397509042(G;G)
Alt rs397509042(G;G)
Reference rs397509042(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244391dupC
CLNSRC ClinVar
CLNACC RCV000048087.2,