{{Rsnum
|rsid=397518448
|Chromosome=1
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AG)
|geno3=(AG;AG)
|Gene=TMCO1
|position=165768765
|Gene_s=RP11-466F5.8,TMCO1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000024096.3
|CLNALLE=1
|CLNDBN=Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3279915:614132
|CLNHGVS=NC_000001.11:g.165768765_165768766delCT
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001256165.1:c.-251_-250delAG; NM_019026.4:c.139_140delAG; NR_045818.1:n.157_158delAG; 614123.0001
|Disease=Craniofacial dysmorphism
|FwdREF=GA
|GENEINFO=RP11-466F5.8:100147773; TMCO1:54499
|GENE_ID=100147773; 54499
|GENE_NAME=RP11-466F5.8; TMCO1
|REF=TCT
|RSPOS=165768764
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSF;REF;U5;R5;ASP;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060421205000002110200
|WGT=1
|dbSNPBuildID=138
|rsid=397518448
|CLNORIGIN=1
}}