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rs141212743

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141212743(C;T)
Make rs141212743(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position12181337
GeneLRP6
is asnp
is mentioned by
dbSNPrs141212743
ebirs141212743
HLIrs141212743
Exacrs141212743
Varsomers141212743
Maprs141212743
PheGenIrs141212743
hapmaprs141212743
1000 genomesrs141212743
hgdprs141212743
ensemblrs141212743
gopubmedrs141212743
geneviewrs141212743
scholarrs141212743
googlers141212743
pharmgkbrs141212743
gwascentralrs141212743
openSNPrs141212743
23andMers141212743
23andMe allrs141212743
SNP Nexus

SNPshotrs141212743
SNPdbers141212743
MSV3drs141212743
GWAS Ctlgrs141212743
Max Magnitude0
ClinVar
Risk rs141212743(T;T)
Alt rs141212743(T;T)
Reference rs141212743(C;C)
Significance Pathogenic
Disease Coronary artery disease
Variation info
Gene LRP6
CLNDBN Coronary artery disease, autosomal dominant 2
Reversed 0
HGVS NC_000012.11:g.12334271C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000056294.2,