| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Familial cardiomyopathy +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hypertrophic cardiomyopathy 3 +1 more | |
Click to view in NCBI Gene