{{Rsnum
|rsid=387906501
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;TCT)
|geno3=(TCT;TCT)
|Gene=SLC16A2
|position=74521020
|Gene_s=SLC16A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000012407.15
|CLNALLE=1
|CLNDBN=Allan-Herndon-Dudley syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK26373:C0795889:300523:59
|CLNHGVS=NC_000023.10:g.73740855_73740857delTCT
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300095.0010
|Disease=Allan-Herndon-Dudley syndrome
|FwdREF=TCT
|REF=ATCT
|RSPOS=73740854
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906501
|GENEINFO=SLC16A2:6567
|GENE_ID=6567
|GENE_NAME=SLC16A2
}}