| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Myopathy, distal, 6, adult-onset, autosomal dominant +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities +3 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +2 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Myopathy, congenital, with structured cores and z-line abnormalities +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Myopathy, congenital, with structured cores and z-line abnormalities +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (synonymous variant) | Primary familial hypertrophic cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1AA +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1AA +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Myopathy, congenital, with structured cores and z-line abnormalities +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1AA +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Myopathy, congenital, with structured cores and z-line abnormalities +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Myopathy, congenital, with structured cores and z-line abnormalities +2 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +7 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | Myopathy, congenital, with structured cores and z-line abnormalities | |
| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Myopathy, congenital, with structured cores and z-line abnormalities +1 more | |
| | | Single nucleotide variant (intron variant) | Myopathy, congenital, with structured cores and z-line abnormalities +1 more | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1AA +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1AA +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Dilated cardiomyopathy 1AA +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1AA +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1AA +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +3 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant +2 more) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Myopathy, congenital, with structured cores and z-line abnormalities +4 more | |
| | | Single nucleotide variant (intron variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Myopathy, congenital, with structured cores and z-line abnormalities +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Myopathy, congenital, with structured cores and z-line abnormalities +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (intron variant) | not provided +7 more | |
| | | Single nucleotide variant (missense variant) | Myopathy, congenital, with structured cores and z-line abnormalities +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +7 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Myopathy, congenital, with structured cores and z-line abnormalities +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1AA +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1AA +6 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1AA +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +10 more | GConflicting classifications of pathogenicity |