| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Myasthenic syndrome, congenital, 24, presynaptic +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | MYO9A-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Myasthenic syndrome, congenital, 24, presynaptic +1 more | |
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