{{Rsnum
|rsid=386833606
|Chromosome=10
|position=124408790
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GAG)
|geno3=(GAG;GAG)
|Gene=OAT
|Gene_s=OAT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=10
|CLNACC=RCV000049533.1
|CLNALLE=1
|CLNDBN=Ornithine aminotransferase deficiency
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0599035:258870:414:276426004
|CLNHGVS=NC_000010.10:g.126097359_126097361delCTC
|CLNSIG=4
|Disease=Ornithine aminotransferase deficiency
|FwdREF=GAG
|REF=ACTC
|RSPOS=126097358
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833606
|GENEINFO=OAT:4942
|GENE_ID=4942
|GENE_NAME=OAT
}}{{PMID Auto
|PMID=8670789
|Title=Heterogeneity and uniqueness of ornithine aminotransferase mutations found in Japanese gyrate atrophy patients.
}}