{{Rsnum
|rsid=387907361
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MED12
|position=71129131
|Gene_s=MED12
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNACC=RCV000043500.22
|CLNALLE=1
|CLNDBN=Ohdo syndrome, X-linked
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN169514:300895:293707
|CLNHGVS=NC_000023.10:g.70348981T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300188.0004
|Disease=Ohdo syndrome
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=70348981
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907361
|GENEINFO=MED12:9968
|GENE_ID=9968
|GENE_NAME=MED12
}}