| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 10 +5 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 10 +5 more | |
Click to view in NCBI Gene