{{Rsnum
|rsid=104894936
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC16A2
|position=74521008
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC16A2
}}{{omim
|id=300095
|rsnum=104894936
|variant=0003
}}{{ClinVar
|rsid=104894936
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=73740843
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SLC16A2:6567
|GENE_NAME=SLC16A2
|GENE_ID=6567
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.73740843C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=9823; 300095.0003
|CLNSIG=5
|CLNCUI=C0795889
|CLNDBN=Allan-Herndon-Dudley syndrome; not provided
|Disease=Allan-Herndon-Dudley syndrome; not provided
|CLNACC=RCV000012400.15; RCV000081445.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK26373:C0795889:300523:59
}}