| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Primary ciliary dyskinesia +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Primary ciliary dyskinesia +10 more | |
Click to view in NCBI Gene