| | | Single nucleotide variant (stop lost +1 more) | Dilated cardiomyopathy 1O +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | Intellectual disability and myopathy syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability and myopathy syndrome +4 more | |
| | | Duplication (frameshift variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O +3 more | |
| | | Deletion (frameshift variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1O +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O +5 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O +5 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability and myopathy syndrome +5 more | |
| | | Single nucleotide variant (intron variant) | Intellectual disability and myopathy syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Hypertrichotic osteochondrodysplasia Cantu type +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrichotic osteochondrodysplasia Cantu type +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 12 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (nonsense) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O +5 more | |
| | | Single nucleotide variant (missense variant) | Hypertrichotic osteochondrodysplasia Cantu type +3 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O +5 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1O +7 more | |
| | | Deletion (frameshift variant) | ABCC9-related disorder +5 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrichotic osteochondrodysplasia Cantu type +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O +5 more | |
| | | Single nucleotide variant (missense variant) | Hypertrichotic osteochondrodysplasia Cantu type +3 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 12 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Dilated cardiomyopathy 1O +4 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrichotic osteochondrodysplasia Cantu type +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Intellectual disability and myopathy syndrome +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1O +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrichotic osteochondrodysplasia Cantu type +3 more | |
| | | Single nucleotide variant (intron variant) | Hypertrichotic osteochondrodysplasia Cantu type +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Intellectual disability and myopathy syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrichotic osteochondrodysplasia Cantu type +3 more | |