{{Rsnum
|rsid=80356528
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=OPA1
|position=193642846
|Gene_s=OPA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356528
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=193360635
|CHROM=3
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=OPA1:4976
|GENE_NAME=OPA1
|GENE_ID=4976
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.193360635G>T
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1248
|CLNSIG=5
|CLNCUI=C0338508
|CLNDBN=Dominant hereditary optic atrophy
|Disease=Dominant hereditary optic atrophy
|CLNACC=RCV000020717.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1248:C0338508:165500:98673:2065009
}}