{{Rsnum
|rsid=67954347
|Chromosome=X
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=OTC
|position=38401367
|Gene_s=OTC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=67954347
|Reversed=0
|FwdREF=T
|FwdALT=A,C,G
|REF=T
|ALT=A,C,G
|RSPOS=38260620
|CHROM=X
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050268000000000002110104
|GENEINFO=OTC:5009
|GENE_NAME=OTC
|GENE_ID=5009
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000023.10:g.38260620T>A; NC_000023.10:g.38260620T>C; NC_000023.10:g.38260620T>G
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM;NOV
|CLNACC=RCV000083451.1; RCV000083452.1; RCV000083453.1
|CLNDBN=not provided
|Disease=not provided
}}

{{PMID Auto
|PMID=11793483
|Title=Identification of seven novel missense mutations, two splice-site mutations, two microdeletions and a polymorphic amino acid substitution in the gene for ornithine transcarbamylase (OTC) in patients with OTC deficiency.
}}

{{PMID Auto
|PMID=16786505
|Title=Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene.
}}

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