{{Rsnum
|rsid=80356531
|Chromosome=3
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=OPA1
|position=193692070
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OPA1
}}{{omim
|id=605290
|rsnum=80356531
|variant=0009
}}{{ClinVar
|rsid=80356531
|Reversed=0
|FwdREF=T
|FwdALT=
|REF=GT
|ALT=G
|RSPOS=193409857
|CHROM=3
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=OPA1:4976
|GENE_NAME=OPA1
|GENE_ID=4976
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.193409859delT
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1248; 605290.0009
|CLNSIG=5
|CLNCUI=C0338508; C0338508
|CLNDBN=Dominant hereditary optic atrophy
|Disease=Dominant hereditary optic atrophy
|CLNACC=RCV000005393.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1248:C0338508:165500:98673:2065009
}}{{PMID Auto
|PMID=11735024
|Title=A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect.
}}