{{Rsnum
|rsid=121918383
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=APOB
|position=21013379
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=APOB
}}{{omim
|id=107730
|rsnum=121918383
|variant=0003
}}{{ClinVar
|rsid=121918383
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=21236251
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=APOB:338
|GENE_NAME=APOB
|GENE_ID=338
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.21236251G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000019472.25
|CLNDBN=Hypobetalipoproteinemia, familial, associated with apob32
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C1862596:60193003
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=107730.0003
|Disease=Hypobetalipoproteinemia
}}