| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Prolonged QT interval +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypertrophic cardiomyopathy +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypertrophic cardiomyopathy 12 +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (nonsense +1 more) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +4 more | |
| | | Deletion (frameshift variant) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 1 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 1 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant | Hypertrophic cardiomyopathy 12 +1 more | |