{{Rsnum
|rsid=121908893
|Gene=SLC22A5
|Chromosome=5
|position=132385435
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC22A5
}}{{omim
|id=603377
|rsnum=121908893
|variant=0019
}}{{ClinVar
|rsid=121908893
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=131721127
|CHROM=5
|GMAF=0.0009
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=SLC22A5:6584
|GENE_NAME=SLC22A5
|GENE_ID=6584
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000005.9:g.131721127C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=3739; 603377.0019
|CLNSIG=5
|CLNCUI=C0342788
|CLNDBN=Renal carnitine transport defect; not provided
|Disease=Renal carnitine transport defect; not provided
|CLNACC=RCV000006795.1; RCV000080059.1
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK84551:C0342788:212140:158:21764004
|COMMON=1
}}