{{Rsnum
|rsid = 28936375
|Gene = CPT2
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=1
|position=53197092
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CPT2
}}{{omim
|desc=CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
|id=600650
|rsnum=28936375
|variant=0003
}}{{ClinVar
|rsid=28936375
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=53197092
|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.53197092C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000098.2:c.149C>A; 600650.0003
|CLNSIG=5
|CLNCUI=C1833508; C1833511
|CLNDBN=CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET; Carnitine palmitoyltransferase II deficiency, infantile
|Disease=CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY; Carnitine palmitoyltransferase II deficiency
|CLNACC=RCV000009511.1; RCV000009512.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1253:C1833508:255110:ORPHA157:ORPHA228302; NBK1253:C1833511:600649:ORPHA228305
}}

{{on chip | 23andMe v4}}