{{Rsnum
|rsid=67501347
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=OTC
|position=38411908
|Gene_s=OTC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=67501347
|Reversed=0
|FwdREF=C
|FwdALT=A,G
|REF=C
|ALT=A,G
|RSPOS=38271161
|CHROM=X
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=OTC:5009
|GENE_NAME=OTC
|GENE_ID=5009
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.38271161C>A; NC_000023.10:g.38271161C>G
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000083608.1; RCV000083609.1
|CLNDBN=not provided
|Disease=not provided
}}

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

{{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.
}}

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