{{Rsnum
|rsid=60376624
|Gene=SLC22A5
|Chromosome=5
|position=132392565
|Orientation=plus
|GMAF=0.0009183
|Gene_s=SLC22A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=G
|CAF=0.9991; 0.0009183
|CHROM=5
|CLNACC=RCV000022379.1; RCV000080050.1
|CLNALLE=1
|CLNDBN=Renal carnitine transport defect; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK84551:C0342788:212140:158:21764004
|CLNHGVS=NC_000005.9:g.131728257C>G
|CLNSIG=5
|COMMON=0
|Disease=Renal carnitine transport defect; not provided
|FwdALT=G
|FwdREF=C
|GENEINFO=SLC22A5:6584
|GENE_ID=6584
|GENE_NAME=SLC22A5
|REF=C
|RSPOS=131728257
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;TPA;PMC;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050078000000000016110100
|WGT=0
|dbSNPBuildID=129
|rsid=60376624
|CLNSRC=Emory University
|CLNSRCID=8449
}}

{{PMID Auto
|PMID=10545605
|Title=Genetic epidemiology of the carnitine transporter OCTN2 gene in a Japanese population and phenotypic characterization in Japanese pedigrees with primary systemic carnitine deficiency.
}}

{{on chip | 23andMe v3}}