| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +2 more) | MYPN-related myopathy | |
| | | Single nucleotide variant (missense variant +1 more) | MYPN-related myopathy +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | MYPN-related myopathy +4 more | |
Click to view in NCBI Gene