{{Rsnum
|rsid=367543059
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC16A2
|position=74529295
|Gene_s=SLC16A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNACC=RCV000034937.1
|CLNALLE=1
|CLNDBN=Allan-Herndon-Dudley syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK26373:C0795889:300523:59
|CLNHGVS=NC_000023.10:g.73749130T>C
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK26373
|Disease=Allan-Herndon-Dudley syndrome
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=73749130
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=367543059
|GENEINFO=SLC16A2:6567
|GENE_ID=6567
|GENE_NAME=SLC16A2
}}