{{Rsnum
|rsid=387906900
|Chromosome=3
|position=193643978
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=OPA1
|Gene_s=OPA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=3
|CLNACC=RCV000023416.1
|CLNALLE=1
|CLNDBN=Optic Atrophy Type 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1248:C1852267:125250:3212
|CLNHGVS=NC_000003.11:g.193361767G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605290.0016
|Disease=Optic Atrophy Type 1
|FwdALT=T
|FwdREF=G
|REF=G
|RSPOS=193361767
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906900
|GENEINFO=OPA1:4976
|GENE_ID=4976
|GENE_NAME=OPA1
}}