{{Rsnum
|rsid=6647476
|Gene=SLC16A2
|Chromosome=X
|position=74421734
|Orientation=plus
|GMAF=0.367
|Gene_s=SLC16A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{PMID Auto
|PMID=23978482
|Title=Associations between single nucleotide polymorphisms in thyroid hormone transporter genes (MCT8, MCT10 and OATP1C1) and circulating thyroid hormones
}}{{ClinVar
|ALT=C
|CAF=0.367; 0.633
|CHROM=X
|CLNACC=RCV000020650.1; RCV000081443.1
|CLNALLE=1
|CLNDBN=Allan-Herndon-Dudley syndrome; AllHighlyPenetrant
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK26373:C0795889:300523:59; CN169374
|CLNHGVS=NC_000023.10:g.73641569T>C
|CLNSIG=2
|CLNSRC=Emory University; GeneReviews
|CLNSRCID=2458; NBK26373
|COMMON=1
|Disease=Allan-Herndon-Dudley syndrome; AllHighlyPenetrant
|FwdALT=C
|FwdREF=T
|GENEINFO=SLC16A2:6567
|GENE_ID=6567
|GENE_NAME=SLC16A2
|REF=T
|RSPOS=73641569
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000100516110100
|WGT=0
|dbSNPBuildID=116
|rsid=6647476
}}{{PMID Auto
|PMID=18710470
|Title=Prevalence and functional analysis of the S107P polymorphism (rs6647476) of the monocarboxylate transporter 8 (SLC16A2) gene in the male population of north-west Spain (Galicia).
}}