| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 8 | |
| | | Single nucleotide variant (splice donor variant) | Hypertrophic cardiomyopathy 8 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Hypertrophic cardiomyopathy 8 +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 8 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 8 +3 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 8 +2 more | |
| | | Indel (frameshift variant +1 more) | Hypertrophic cardiomyopathy 8 +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +2 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 8 +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 8 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hypertrophic cardiomyopathy 8 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 8 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 8 | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 8 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 8 +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 8 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 8 +4 more | |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 8 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 8 +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |