{{Rsnum
|rsid=386134225
|Chromosome=5
|position=132393784
|Orientation=plus
|geno1=(-;-)
|geno2=(-;ACAC)
|geno3=(ACAC;ACAC)
|Gene=SLC22A5
|Gene_s=SLC22A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GACAC
|CHROM=5
|CLNACC=RCV000022387.1
|CLNALLE=1
|CLNDBN=Renal carnitine transport defect
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK84551:C0342788:212140:158:21764004
|CLNHGVS=NC_000005.9:g.131729473_131729476dupACAC
|CLNSIG=5
|Disease=Renal carnitine transport defect
|FwdALT=ACAC
|REF=G
|RSPOS=131729472
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386134225
|GENEINFO=SLC22A5:6584
|GENE_ID=6584
|GENE_NAME=SLC22A5
}}{{PMID Auto
|PMID=17126586
|Title=Expanded newborn screening identifies maternal primary carnitine deficiency.
}}