{{Rsnum
|rsid=104894940
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=SLC16A2
|position=74525844
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC16A2
}}{{omim
|id=300095
|rsnum=104894940
|variant=0009
}}{{ClinVar
|rsid=104894940
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=73745679
|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.73745679C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300095.0009
|CLNSIG=5
|CLNCUI=C0795889
|CLNDBN=Allan-Herndon-Dudley syndrome
|Disease=Allan-Herndon-Dudley syndrome
|CLNACC=RCV000012406.21
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK26373:C0795889:300523:59
}}