| | | Single nucleotide variant (nonsense) | Dilated cardiomyopathy 2A +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +3 more | |
| | DNAAF3, DNAAF3-AS1 +1 more (R108S +3 more) | Single nucleotide variant (missense variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +4 more | |
| | DNAAF3, DNAAF3-AS1 +2 more | Single nucleotide variant (synonymous variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +6 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +5 more | |
| | | Duplication (frameshift variant) | Hypertrophic cardiomyopathy 7 +6 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +5 more | |
| | | Single nucleotide variant (splice donor variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy, familial restrictive, 1 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +6 more | |
| | DNAAF3, DNAAF3-AS1 +1 more | Single nucleotide variant (synonymous variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy, familial restrictive, 1 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy, familial restrictive, 1 +5 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +6 more | |
| | | Single nucleotide variant (nonsense) | Hypertrophic cardiomyopathy +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1FF +7 more | |
| | | Deletion (frameshift variant) | Myocarditis +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 2A +6 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Familial restrictive cardiomyopathy +8 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 7 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 2A +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 7 +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +11 more | |
| | | Single nucleotide variant (synonymous variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +9 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +10 more | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy, familial restrictive, 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +9 more | |
| | | Single nucleotide variant (intron variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 7 +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified +12 more | |