| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | DNAAF3, DNAAF3-AS1
+1 more (H386Q +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | DNAAF3, DNAAF3-AS1
+2 more (L381P +3 more) | Single nucleotide variant (missense variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +6 more | |
| | DNAAF3, DNAAF3-AS1
+1 more (T398I +3 more) | Single nucleotide variant (missense variant) | DNAAF3-related condition +2 more | |
| | DNAAF3, DNAAF3-AS1
+1 more (T377A +3 more) | Single nucleotide variant (missense variant) | Primary ciliary dyskinesia | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene