{{Rsnum
|rsid = 28934611
|Gene = MID1
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=X
|position=10449495
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MID1
}}{{omim
|desc=OPITZ SYNDROME, X-LINKED
|id=300552
|rsnum=28934611
|variant=0004
}}

{{ClinVar
|rsid=28934611
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=10417535
|CHROM=X
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MID1:4281
|GENE_NAME=MID1
|GENE_ID=4281
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.10417535A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300552.0004
|CLNSIG=5
|CLNCUI=C0175696
|CLNDBN=Opitz-Frias syndrome
|Disease=Opitz-Frias syndrome
|CLNACC=RCV000011555.6
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1327:C0175696:300000:2745:81771002
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}