{{Rsnum
|rsid=74315298
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CPT2
|position=53210354
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CPT2
}}{{omim
|id=600650
|rsnum=74315298
|variant=0013
}}{{ClinVar
|rsid=74315298
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=53210354
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05040002110100
|GENEINFO=CPT2:1376
|GENE_NAME=CPT2
|GENE_ID=1376
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.53210354C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000098.2:c.680C>T; 600650.0013
|CLNSIG=5
|CLNCUI=C1833518
|CLNDBN=CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
|Disease=CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY
|CLNACC=RCV000009526.1
|Tags=PM;S3D;NSM;REF;ASP;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1253:C1833518:608836:ORPHA228308
}}