{{Rsnum
|rsid=80356524
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OPA3
|position=45553777
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OPA3
}}{{omim
|id=606580
|rsnum=80356524
|variant=0002
}}{{ClinVar
|rsid=80356524
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=46057035
|CHROM=19
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=OPA3:80207
|GENE_NAME=OPA3
|GENE_ID=80207
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.46057035C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1473; 606580.0002
|CLNSIG=5
|CLNCUI=C1833809; C1833809
|CLNDBN=Optic atrophy and cataract, autosomal dominant
|Disease=Optic atrophy and cataract
|CLNACC=RCV000004462.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1473:C1833809:165300:67036
}}{{PMID Auto
|PMID=13703570
|Title=[On a heredo-familial disease combining cataract, optic atrophy, extrapyramidal symptoms and certain defects of Friedreich's disease. (Its nosological position in relation to the Behr's syndrome, the Marinesco-Sjogren syndrome and Friedreich's disease with ocular symptoms].
}}

{{PMID Auto
|PMID=15342707
|Title=OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract.
|OA=1
}}