{{Rsnum
|rsid=137852912
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PCSK9
|position=55057454
|Gene_s=PCSK9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=607786
|variant=0003
|rsnum=137852912
}}{{ClinVar
|rsid=137852912
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=55057454
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=PCSK9:255738
|GENE_NAME=PCSK9
|GENE_ID=255738
|WGT=1
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000001.11:g.55057454G>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_174936.3:c.1120G>T; NR_110451.1:n.779G>T; 607786.0003
|CLNSIG=5
|CLNCUI=C1863551
|CLNDBN=Hypercholesterolemia, autosomal dominant, 3
|Disease=Hypercholesterolemia
|CLNACC=RCV000003009.2
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1863551:603776
}}