| | | Duplication | Hypertrophic cardiomyopathy 16 +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 16 +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +4 more | |
| | | Single nucleotide variant (nonsense) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 16 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cardiomyopathy | |