| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant +1 more) | Hypertrophic cardiomyopathy 10 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant +1 more) | Hypertrophic cardiomyopathy 10 +1 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene