{{Rsnum
|rsid=121918528
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CPT2
|position=53210033
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CPT2
}}{{omim
|id=600650
|rsnum=121918528
|variant=0017
}}{{ClinVar
|rsid=121918528
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=53210033
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=CPT2:1376
|GENE_NAME=CPT2
|GENE_ID=1376
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.53210033A>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000098.2:c.359A>G; 600650.0017
|CLNSIG=5
|CLNCUI=C1833511
|CLNDBN=Carnitine palmitoyltransferase II deficiency, infantile
|Disease=Carnitine palmitoyltransferase II deficiency
|CLNACC=RCV000009530.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1253:C1833511:600649:ORPHA228305
}}