{{Rsnum
|rsid=121908376
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OPA1
|position=193648109
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OPA1
}}{{omim
|id=605290
|rsnum=121908376
|variant=0013
}}{{ClinVar
|rsid=121908376
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=193365898
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=OPA1:4976
|GENE_NAME=OPA1
|GENE_ID=4976
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.193365898A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605290.0013
|CLNSIG=5
|CLNCUI=C1852267
|CLNDBN=Optic Atrophy Type 1
|Disease=Optic Atrophy Type 1
|CLNACC=RCV000005395.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1248:C1852267:125250:3212
}}