| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | Hypertrophic cardiomyopathy 25 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +7 more | |
Click to view in NCBI Gene