| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | 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 | |
| | | 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 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | 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 (stop lost +1 more) | Hypertrophic cardiomyopathy 12 | |
| | | Single nucleotide variant (missense variant +1 more) | CSRP3-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | | Microsatellite (frameshift variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1M +3 more | |
| | | Deletion (frameshift variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +3 more | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (missense variant) | CSRP3-related disorder +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Duplication (frameshift variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Microsatellite (splice acceptor variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 12 +4 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Duplication (intron variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (splice donor variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +3 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1M +1 more | |
| | | Duplication (frameshift variant) | Hypertrophic cardiomyopathy 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1M +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | |
| | | Deletion (frameshift variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Microsatellite (frameshift variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypertrophic cardiomyopathy 12 +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +2 more | |
| | | Single nucleotide variant (missense variant) | Prolonged QT interval +5 more | |