| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | OPA1, OPA1-AS1 (A192V +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal dominant optic atrophy classic form +2 more | |
| | | Single nucleotide variant (intron variant) | OPA1-related condition +2 more | |
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