{{Rsnum
|rsid = 28936673
|Gene = CPT2
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=C
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=1
|position=53213501
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CPT2
}}{{omim
|desc=CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
|id=600650
|rsnum=28936673
|variant=0005
}}

{{ClinVar
|rsid=28936673
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=53213501
|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.53213501A>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000098.2:c.1883A>C; 600650.0005
|CLNSIG=5
|CLNCUI=C1833511; C1833508
|CLNDBN=Carnitine palmitoyltransferase II deficiency, infantile; CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
|Disease=Carnitine palmitoyltransferase II deficiency; CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY
|CLNACC=RCV000009514.3; RCV000009515.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1253:C1833511:600649:ORPHA228305; NBK1253:C1833508:255110:ORPHA157:ORPHA228302
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}