| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 10 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Primary familial hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Microsatellite (frameshift variant) | Dilated cardiomyopathy 1BB +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ventricular fibrillation | |
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