{{Rsnum
|rsid=104893753
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OPA1
|position=193643005
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OPA1
}}{{omim
|id=605290
|rsnum=104893753
|variant=0006
}}{{ClinVar
|rsid=104893753
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=193360794
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=OPA1:4976
|GENE_NAME=OPA1
|GENE_ID=4976
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.193360794C>T
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=7550; 605290.0006
|CLNSIG=5
|CLNCUI=C0338508; C0338508
|CLNDBN=Dominant hereditary optic atrophy; not provided
|Disease=Dominant hereditary optic atrophy; not provided
|CLNACC=RCV000005390.1; RCV000081746.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1248:C0338508:165500:98673:2065009
}}