{{Rsnum
|rsid=387906719
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MID1
|position=10523136
|Gene_s=MID1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000022867.3
|CLNALLE=1
|CLNDBN=Opitz-Frias syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1327:C0175696:300000:2745:81771002
|CLNHGVS=NC_000023.10:g.10491176C>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300552.0009
|Disease=Opitz-Frias syndrome
|FwdALT=T
|FwdREF=G
|REF=C
|RSPOS=10491176
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906719
|GENEINFO=MID1:4281
|GENE_ID=4281
|GENE_NAME=MID1
}}