{{Rsnum
|rsid=201213306
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TMCO1
|position=165752166
|Gene_s=TMCO1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000074398.2
|CLNALLE=1
|CLNDBN=Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3279915:614132
|CLNHGVS=NC_000001.11:g.165752166G>A
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_019026.4:c.412C>T; 614123.0002
|Disease=Craniofacial dysmorphism
|FwdALT=A
|FwdREF=G
|GENEINFO=TMCO1:54499
|GENE_ID=54499
|GENE_NAME=TMCO1
|REF=G
|RSPOS=165752166
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSN;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000605000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=201213306
|CLNORIGIN=1
}}