{{Rsnum
|rsid=11568514
|Gene=SLC22A5
|Chromosome=5
|position=132392510
|Orientation=plus
|GMAF=0.0004591
|Gene_s=SLC22A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 1.6 | 98.4
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{ClinVar
|ALT=G
|CAF=0.9995; 0.0004591
|CHROM=5
|CLNACC=RCV000022376.1; RCV000080049.1
|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.131728202T>G
|CLNSIG=5
|COMMON=0
|Disease=Renal carnitine transport defect; not provided
|FwdALT=G
|FwdREF=T
|GENEINFO=SLC22A5:6584
|GENE_ID=6584
|GENE_NAME=SLC22A5
|REF=T
|RSPOS=131728202
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;TPA;PMC;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x050178000000040517110100
|WGT=0
|dbSNPBuildID=127
|rsid=11568514
|CLNSRC=Emory University
|CLNSRCID=14884
}}

{{ population diversity
| geno1 = (G;T)
| geno2 = (T;T)
| geno3 = 
| CEU | 0.0 | 100.0 | 0
| HCB | 0.0 | 100.0 | 0
| JPT | 0.0 | 100.0 | 0
| YRI | 1.7 | 98.3 | 0
| ASW | 0 | 0 | 0
| CHD | 0 | 0 | 0
| GIH | 0 | 0 | 0
| LWK | 0 | 0 | 0
| MEX | 0 | 0 | 0
| MKK | 0 | 0 | 0
| TSI | 0 | 0 | 0
}}

{{PMID Auto
|PMID=14665638
|Title=Tyrosine residues affecting sodium stimulation of carnitine transport in the OCTN2 carnitine/organic cation transporter.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}