| | | Single nucleotide variant (missense variant) | Desmin-related myofibrillar myopathy +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (synonymous variant) | Neurogenic scapuloperoneal syndrome, Kaeser type +6 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1I +2 more | |
| | | Single nucleotide variant (missense variant) | Neurogenic scapuloperoneal syndrome, Kaeser type +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Dilated cardiomyopathy 1I +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Neurogenic scapuloperoneal syndrome, Kaeser type +2 more | |
| | | Single nucleotide variant (nonsense) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Desmin-related myofibrillar myopathy +2 more | |
| | | Single nucleotide variant (missense variant) | Desmin-related myofibrillar myopathy +20 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Desmin-related myofibrillar myopathy +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1I +3 more | |
| | | Single nucleotide variant (nonsense) | Neurogenic scapuloperoneal syndrome, Kaeser type +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Desmin-related myofibrillar myopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1I +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1I +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1I +4 more | |
| | | Single nucleotide variant (missense variant) | Neurogenic scapuloperoneal syndrome, Kaeser type +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +7 more | |
| | | Single nucleotide variant (missense variant) | Desmin-related myofibrillar myopathy +2 more | |
| | | Single nucleotide variant (nonsense +1 more) | Desmin-related myofibrillar myopathy +3 more | GPathogenic/Likely pathogenic |
| | | Deletion | not provided +10 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1I +5 more | |
| | | Single nucleotide variant (missense variant) | Desmin-related myofibrillar myopathy +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1I +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Desmin-related myofibrillar myopathy +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Desmin-related myofibrillar myopathy +4 more | |
| | | Indel (missense variant +1 more) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Neurogenic scapuloperoneal syndrome, Kaeser type +5 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1I +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1I +5 more | |
| | | Single nucleotide variant (missense variant) | Neurogenic scapuloperoneal syndrome, Kaeser type +4 more | |
| | | Single nucleotide variant (missense variant) | Desmin-related myofibrillar myopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Desmin-related myofibrillar myopathy +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (splice donor variant) | Desmin-related myofibrillar myopathy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1I +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1I +2 more | |