{{Rsnum
|rsid = 28942112
|Gene = PCSK9
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=1
|position=55052400
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PCSK9
}}{{omim
|desc=HYPERCHOLESTEROLEMIA, FAMILIAL, 3
|id=607786
|rsnum=28942112
|variant=0002
}}{{ClinVar
|rsid=28942112
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=55052400
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=PCSK9:255738
|GENE_NAME=PCSK9
|GENE_ID=255738
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.55052400T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_174936.3:c.646T>C; NR_110451.1:n.305T>C; 607786.0002
|CLNSIG=5
|CLNCUI=C1863551
|CLNDBN=Hypercholesterolemia, autosomal dominant, 3
|Disease=Hypercholesterolemia
|CLNACC=RCV000003008.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1863551:603776
}}