{{Rsnum
|rsid=72554338
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OTC
|position=38369838
|Gene_s=OTC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=72554338
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=38229091
|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
|CLNHGVS=NC_000023.10:g.38229091G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=300461.0016
|CLNSIG=5
|CLNCUI=C0268542
|CLNDBN=Ornithine carbamoyltransferase deficiency; not provided
|Disease=Ornithine carbamoyltransferase deficiency; not provided
|CLNACC=RCV000011748.4; RCV000083376.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK154378:C0268542:311250:664:80908008
}}

{{PMID Auto
|PMID=1353535
|Title=Site specific screening for point mutations in ornithine transcarbamylase deficiency.
|OA=1
}}

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