| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | CSRP3-related disorder +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 12 +6 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | CSRP3-related disorder | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 12 +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GConflicting classifications of pathogenicity |
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