{{Rsnum
|rsid=121918313
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LRP6
|position=12164494
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LRP6
}}{{omim
|id=603507
|rsnum=121918313
|variant=0001
}}{{ClinVar
|rsid=121918313
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=12317428
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=LRP6:4040
|GENE_NAME=LRP6
|GENE_ID=4040
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.12317428G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603507.0001
|CLNSIG=5
|CLNCUI=C1970440
|CLNDBN=Coronary artery disease, autosomal dominant 2
|Disease=Coronary artery disease
|CLNACC=RCV000006645.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1970440:610947:94062
}}