{{Rsnum
|rsid=67468335
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OTC
|position=38411901
|Gene_s=OTC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=67468335
|Reversed=0
|FwdREF=T
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=38271154
|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.38271154T>C; NC_000023.10:g.38271154T>G
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000083604.1; RCV000083605.1
|CLNDBN=not provided
|Disease=not provided
}}

{{PMID Auto
|PMID=9452049
|Title=Novel intragenic deletions and point mutations of the ornithine transcarbamylase gene in congenital hyperammonemia.
}}

{{PMID Auto
|PMID=11793468
|Title=Mutations and polymorphisms in the human ornithine transcarbamylase gene.
}}

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