{{Rsnum
|rsid=387906899
|Chromosome=3
|position=193643609
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OPA1
|Gene_s=OPA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=3
|CLNACC=RCV000023414.1
|CLNALLE=1
|CLNDBN=Optic Atrophy Type 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1248:C1852267:125250:3212
|CLNHGVS=NC_000003.11:g.193361398A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605290.0014
|Disease=Optic Atrophy Type 1
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=193361398
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906899
|GENEINFO=OPA1:4976
|GENE_ID=4976
|GENE_NAME=OPA1
}}