{{Rsnum
|rsid=1800456
|Chromosome=10
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=OAT
|position=124397951
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OAT
}}{{omim
|id=613349
|rsnum=1800456
|variant=0013
}}{{ClinVar
|rsid=1800456
|Reversed=1
|FwdREF=G
|FwdALT=C,T
|REF=C
|ALT=A,G
|RSPOS=126086520
|CHROM=10
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050368000000040102110100
|GENEINFO=OAT:4942
|GENE_NAME=OAT
|GENE_ID=4942
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.126086520C>A
|CLNORIGIN=1
|CLNSIG=4
|Tags=RV;PM;PMC;S3D;SLO;VLD;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000049525.1
|CLNDBN=Ornithine aminotransferase deficiency
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0599035:258870:414:276426004
|Disease=Ornithine aminotransferase deficiency
}}{{PMID Auto
|PMID=23076989
|Title=Functional analysis of missense mutations of OAT, causing gyrate atrophy of choroid and retina.
}}