{{Rsnum
|rsid=120074112
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=APOC2
|position=44948479
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=APOC2,INPP4B
}}{{omim
|id=608083
|rsnum=120074112
|variant=0007
}}{{ClinVar
|rsid=120074112
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=45451736
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=APOC2:344; APOC4-APOC2:100533990
|GENE_NAME=APOC2; APOC4-APOC2
|GENE_ID=344; 100533990
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.45451736A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608083.0007
|CLNSIG=5
|CLNCUI=C1720779
|CLNDBN=APOLIPOPROTEIN C-II (PARIS); Apolipoprotein C2 deficiency
|Disease=APOLIPOPROTEIN C-II (PARIS); Apolipoprotein C2 deficiency
|CLNACC=RCV000002693.1; RCV000002694.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1720779:207750:411
}}