{{Rsnum
|rsid=386833609
|Chromosome=10
|position=124408634
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GATAGGAGT)
|geno3=(GATAGGAGT;GATAGGAGT)
|Gene=OAT
|Gene_s=OAT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=10
|CLNACC=RCV000049536.1
|CLNALLE=1
|CLNDBN=Ornithine aminotransferase deficiency
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0599035:258870:414:276426004
|CLNHGVS=NC_000010.10:g.126097203_126097211delACTCCTATC
|CLNSIG=4
|Disease=Ornithine aminotransferase deficiency
|FwdREF=ATAGGAGTG
|REF=CACTCCTATC
|RSPOS=126097202
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833609
|GENEINFO=OAT:4942
|GENE_ID=4942
|GENE_NAME=OAT
}}{{PMID Auto
|PMID=2220818
|Title=Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophy.
|OA=1
}}