{{Rsnum
|rsid=121965044
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OAT
|position=124398012
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OAT
}}{{omim
|id=613349
|rsnum=121965044
|variant=0012
}}{{ClinVar
|rsid=121965044
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=126086581
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=OAT:4942
|GENE_NAME=OAT
|GENE_ID=4942
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.126086581G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613349.0012
|CLNSIG=255
|CLNCUI=CN030190
|CLNDBN=Ornithine aminotransferase deficiency
|Disease=Ornithine aminotransferase deficiency
|CLNACC=RCV000000180.3
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0599035:258870:414:276426004
}}{{PMID Auto
|PMID=23076989
|Title=Functional analysis of missense mutations of OAT, causing gyrate atrophy of choroid and retina.
}}