{{Rsnum
|rsid=113994166
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=SLC16A2
|position=74531545
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC16A2
}}{{omim
|id=300095
|rsnum=113994166
|variant=0011
}}{{ClinVar
|rsid=113994166
|Reversed=0
|FwdREF=C
|FwdALT=
|REF=AC
|ALT=A
|RSPOS=73751379
|CHROM=X
|dbSNPBuildID=137
|SSR=0
|SAO=0
|VP=0x050160000000000002110200
|GENEINFO=SLC16A2:6567
|GENE_NAME=SLC16A2
|GENE_ID=6567
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.73751380delC
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK26373; 300095.0011
|CLNSIG=5
|CLNCUI=C0795889; C0795889
|CLNDBN=Allan-Herndon-Dudley syndrome
|Disease=Allan-Herndon-Dudley syndrome
|CLNACC=RCV000012408.15
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK26373:C0795889:300523:59
}}