| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (splice acceptor variant) | Ciliary dyskinesia, primary, 40 | |
| | | Deletion (frameshift variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (nonsense) | Ciliary dyskinesia, primary, 40 | |
| | DNAH9, LOC101928350 (T3647S) | Single nucleotide variant (missense variant +1 more) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | | Single nucleotide variant (missense variant) | DNAH9-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Deletion (frameshift variant) | Ciliary dyskinesia, primary, 40 | |
| | | Deletion (frameshift variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | DNAH9, LOC126862506 (R1640*) | Single nucleotide variant (nonsense) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (nonsense) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (synonymous variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | DNAH9, LOC101928350 (T3618M) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | | Single nucleotide variant (missense variant) | DNAH9-related condition +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | DNAH9-related condition +2 more | |
| | | Single nucleotide variant (intron variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | | Microsatellite (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Deletion (frameshift variant) | Ciliary dyskinesia, primary, 40 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | DNAH9, LOC101928350 (T3487R) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | | Single nucleotide variant (nonsense) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (nonsense) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (nonsense) | Ciliary dyskinesia, primary, 40 | |
| | | Deletion (frameshift variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (intron variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | | Single nucleotide variant (intron variant) | Ciliary dyskinesia, primary, 40 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (nonsense) | Ciliary dyskinesia, primary, 40 | |
| | | Deletion (intron variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (synonymous variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Duplication (frameshift variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (splice acceptor variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (nonsense) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 | |
| | | Duplication (frameshift variant) | Ciliary dyskinesia, primary, 40 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Abnormal cardiovascular system morphology +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (intron variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (missense variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Ciliary dyskinesia, primary, 40 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Ciliary dyskinesia, primary, 40 +2 more | |