{{Rsnum
|rsid = 28939082
|Gene = OPA1
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=3
|position=193637980
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OPA1
}}{{omim
|desc=OPTIC ATROPHY 1
|id=605290
|rsnum=28939082
|variant=0001
}}

{{ClinVar
|rsid=28939082
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=193355769
|CHROM=3
|dbSNPBuildID=133
|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.193355769G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605290.0001
|CLNSIG=5
|CLNCUI=C0338508
|CLNDBN=Dominant hereditary optic atrophy
|Disease=Dominant hereditary optic atrophy
|CLNACC=RCV000005385.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1248:C0338508:165500:98673:2065009
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}