{{Rsnum
|rsid=121908892
|Chromosome=5
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SLC22A5
|position=132369975
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MIR4750,SLC22A5
}}{{omim
|id=603377
|rsnum=121908892
|variant=0018
}}{{ClinVar
|rsid=121908892
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=131705667
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=LOC553103:553103; SLC22A5:6584
|GENE_NAME=LOC553103; SLC22A5
|GENE_ID=553103; 6584
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.131705667G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603377.0018
|CLNSIG=5
|CLNCUI=C0342788
|CLNDBN=Renal carnitine transport defect
|Disease=Renal carnitine transport defect
|CLNACC=RCV000006794.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK84551:C0342788:212140:158:21764004
}}