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rs397515473

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515473(A;G)
Make rs397515473(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position12181118
GeneLRP6
is asnp
is mentioned by
dbSNPrs397515473
ebirs397515473
HLIrs397515473
Exacrs397515473
Varsomers397515473
Maprs397515473
PheGenIrs397515473
hapmaprs397515473
1000 genomesrs397515473
hgdprs397515473
ensemblrs397515473
gopubmedrs397515473
geneviewrs397515473
scholarrs397515473
googlers397515473
pharmgkbrs397515473
gwascentralrs397515473
openSNPrs397515473
23andMers397515473
23andMe allrs397515473
SNP Nexus

SNPshotrs397515473
SNPdbers397515473
MSV3drs397515473
GWAS Ctlgrs397515473
Max Magnitude0
ClinVar
Risk rs397515473(G;G)
Alt rs397515473(G;G)
Reference rs397515473(A;A)
Significance Pathogenic
Disease Coronary artery disease
Variation info
Gene LRP6
CLNDBN Coronary artery disease, autosomal dominant 2
Reversed 1
HGVS NC_000012.11:g.12334052T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000056292.2,