| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1Y +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 3 | |
| | | Single nucleotide variant (missense variant +2 more) | Dilated cardiomyopathy 1Y +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 3 | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 3 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 3 +2 more | |
| | | Insertion (3 prime UTR variant +2 more) | Hypertrophic cardiomyopathy 3 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1Y +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hypertrophic cardiomyopathy 3 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 3 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 3 | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 3 | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy +1 more | |
| | | Single nucleotide variant (intron variant +1 more) | Dilated cardiomyopathy 1Y +4 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Dilated cardiomyopathy 1Y +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 3 +2 more | |
| | | Single nucleotide variant (intron variant +1 more) | Cardiomyopathy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hypertrophic cardiomyopathy 3 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Hypertrophic cardiomyopathy 3 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Hypertrophic cardiomyopathy 3 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Hypertrophic cardiomyopathy 3 +1 more | |
| | | Single nucleotide variant | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Dilated cardiomyopathy 1Y +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 3 +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 3 | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1Y +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 3 +3 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1Y +3 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 3 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hypertrophic cardiomyopathy 3 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Dilated cardiomyopathy 1Y +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Hypertrophic cardiomyopathy 3 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Hypertrophic cardiomyopathy 3 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1Y +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant | Dilated cardiomyopathy 1Y +1 more | |
| | | Single nucleotide variant | Hypertrophic cardiomyopathy 3 +2 more | |
| | | Single nucleotide variant | Hypertrophic cardiomyopathy 3 +1 more | |
| | | Single nucleotide variant | Dilated cardiomyopathy 1Y +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | See cases +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 3 +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1Y +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dilated cardiomyopathy 1Y +4 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial cardiomyopathy +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 3 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (nonsense +1 more) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +6 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +7 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |