| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Myopathy, proximal, and ophthalmoplegia | |
| | | Single nucleotide variant (missense variant) | Myopathy, proximal, and ophthalmoplegia | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Myopathy, proximal, and ophthalmoplegia | |
Click to view in NCBI Gene