| | | Single nucleotide variant (3 prime UTR variant) | not specified | |
| | | Duplication (intron variant) | not specified +2 more | |
| | | Deletion (intron variant) | Intellectual disability and myopathy syndrome +3 more | |
| | | Deletion (intron variant) | Primary dilated cardiomyopathy +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1O | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1O +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrichotic osteochondrodysplasia Cantu type +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant +1 more) | Cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | ABCC9-related disorder +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Conduction disorder of the heart +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1O | |
| | | Single nucleotide variant (synonymous variant) | ABCC9-related disorder +6 more | |
| | | Single nucleotide variant (synonymous variant) | ABCC9-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (no sequence alteration) | not specified +4 more | |
| | | Deletion (intron variant) | Dilated Cardiomyopathy, Dominant +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1O +2 more | |
| | | Deletion (intron variant) | not specified +3 more | |
| | | Duplication (intron variant) | not specified +1 more | |
| | | Deletion (intron variant) | Dilated cardiomyopathy 1O +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Duplication (intron variant) | not specified +1 more | |