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rs121918313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918313(C;T)
Make rs121918313(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position12164494
GeneLRP6
is asnp
is mentioned by
dbSNPrs121918313
ebirs121918313
HLIrs121918313
Exacrs121918313
Varsomers121918313
Maprs121918313
PheGenIrs121918313
hapmaprs121918313
1000 genomesrs121918313
hgdprs121918313
ensemblrs121918313
gopubmedrs121918313
geneviewrs121918313
scholarrs121918313
googlers121918313
pharmgkbrs121918313
gwascentralrs121918313
openSNPrs121918313
23andMers121918313
23andMe allrs121918313
SNP Nexus

SNPshotrs121918313
SNPdbers121918313
MSV3drs121918313
GWAS Ctlgrs121918313
Max Magnitude0
OMIM603507
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918313(T;T)
Alt rs121918313(T;T)
Reference Rs121918313(C;C)
Significance Pathogenic
Disease Coronary artery disease
Variation info
Gene LRP6
CLNDBN Coronary artery disease, autosomal dominant 2
Reversed 1
HGVS NC_000012.11:g.12317428G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000006645.3,