| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Myofibrillar myopathy 3 +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | MYOT-related disorder +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene