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rs397515474

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515474(A;A)
Make rs397515474(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position12179937
GeneLRP6
is asnp
is mentioned by
dbSNPrs397515474
ebirs397515474
HLIrs397515474
Exacrs397515474
Varsomers397515474
Maprs397515474
PheGenIrs397515474
hapmaprs397515474
1000 genomesrs397515474
hgdprs397515474
ensemblrs397515474
gopubmedrs397515474
geneviewrs397515474
scholarrs397515474
googlers397515474
pharmgkbrs397515474
gwascentralrs397515474
openSNPrs397515474
23andMers397515474
23andMe allrs397515474
SNP Nexus

SNPshotrs397515474
SNPdbers397515474
MSV3drs397515474
GWAS Ctlgrs397515474
Max Magnitude0
ClinVar
Risk rs397515474(A;A)
Alt rs397515474(A;A)
Reference rs397515474(G;G)
Significance Pathogenic
Disease Coronary artery disease
Variation info
Gene LRP6
CLNDBN Coronary artery disease, autosomal dominant 2
Reversed 1
HGVS NC_000012.11:g.12332871C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000056293.2,