| | | Single nucleotide variant (3 prime UTR variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +5 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +3 more | |
| | | Insertion (frameshift variant) | Cardiomyopathy | |
| | | Duplication (frameshift variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | not specified +6 more | |
| | | Deletion (frameshift variant) | Hypertrophic cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 10 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 10 +1 more | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 10 +1 more | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Primary familial hypertrophic cardiomyopathy +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Duplication (frameshift variant) | Cardiomyopathy | |
| | | Deletion (frameshift variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | Deletion (frameshift variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (splice acceptor variant) | Cardiomyopathy | |
| | | Single nucleotide variant (splice acceptor variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Deletion (frameshift variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Hypertrophic cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiomyopathy | |
| | | Microsatellite (intron variant) | Cardiomyopathy +2 more | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 10 +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity |