{{Rsnum
|rsid=386833604
|Chromosome=10
|position=124408854
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OAT
|Gene_s=OAT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=C
|CHROM=10
|CLNACC=RCV000049531.1
|CLNALLE=1
|CLNDBN=Ornithine aminotransferase deficiency
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0599035:258870:414:276426004
|CLNHGVS=NC_000010.10:g.126097423T>C
|CLNSIG=4
|Disease=Ornithine aminotransferase deficiency
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=126097423
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833604
|GENEINFO=OAT:4942
|GENE_ID=4942
|GENE_NAME=OAT
}}{{PMID Auto
|PMID=23076989
|Title=Functional analysis of missense mutations of OAT, causing gyrate atrophy of choroid and retina.
}}