| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 10 +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +4 more | |
| | | Single nucleotide variant (nonsense) | Hypertrophic cardiomyopathy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +5 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +3 more | |
| | | Single nucleotide variant (missense variant) | Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 10 +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | |