| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +2 more | |
| | | Single nucleotide variant (intron variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +9 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene