| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +2 more) | Primary familial hypertrophic cardiomyopathy +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Dilated cardiomyopathy 1KK +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | Left ventricular noncompaction cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Primary familial hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Primary familial hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1KK +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1KK +3 more | GConflicting classifications of pathogenicity |
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