{{Rsnum
|rsid=138350727
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=OPA1
|position=193626153
|Gene_s=OPA1,OPA1-AS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=3
|CLNACC=RCV000055988.1
|CLNALLE=1
|CLNDBN=Dominant hereditary optic atrophy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1248:C0338508:165500:98673:2065009
|CLNHGVS=NC_000003.11:g.193343942G>A
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1248
|Disease=Dominant hereditary optic atrophy
|FwdALT=A,T
|FwdREF=G
|GENEINFO=OPA1:4976; OPA1-AS1:100873941
|GENE_ID=4976; 100873941
|GENE_NAME=OPA1; OPA1-AS1
|REF=G
|RSPOS=193343942
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=138350727
}}