{{Rsnum
|rsid=74315299
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CPT2
|position=53211034
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CPT2
}}{{omim
|id=600650
|rsnum=74315299
|variant=0015
}}{{ClinVar
|rsid=74315299
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=53211034
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=CPT2:1376
|GENE_NAME=CPT2
|GENE_ID=1376
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.53211034G>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000098.2:c.1360G>T; 600650.0015
|CLNSIG=5
|CLNCUI=C1833508
|CLNDBN=CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
|Disease=CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY
|CLNACC=RCV000009528.3
|Tags=PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1253:C1833508:255110:ORPHA157:ORPHA228302
}}