{{Rsnum
|rsid=80356523
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=OPA3
|position=45553912
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OPA3
}}{{omim
|id=606580
|rsnum=80356523
|variant=0001
}}{{ClinVar
|rsid=80356523
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=46057170
|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.46057170C>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1473; 606580.0001
|CLNSIG=5
|CLNCUI=C0574084; C0574084
|CLNDBN=3-Methylglutaconic aciduria type 3
|Disease=3-Methylglutaconic aciduria type 3
|CLNACC=RCV000004461.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1473:C0574084:258501:67047:297232009
}}{{PMID Auto
|PMID=11668429
|Title=Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews.
|OA=1
}}