| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Myofibrillar myopathy 3 +11 more | GPathogenic/Likely pathogenic |
| | MYOT, PKD2L2-DT (T333I +2 more) | Single nucleotide variant (missense variant) | Myofibrillar myopathy 3 +2 more | |
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