| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Indel (inframe_indel) | WDR26-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | WDR26-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | WDR26-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (frameshift variant) | Skraban-Deardorff syndrome | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | Intellectual disability | |
| | | Deletion (nonsense) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication (frameshift variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (nonsense) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Seizure | |
| | | Single nucleotide variant (missense variant) | WDR26-related disorder | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Skraban-Deardorff syndrome | |
| | | Deletion (inframe_deletion) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Deletion (frameshift variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (synonymous variant) | WDR26-related disorder | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Deletion (frameshift variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (splice donor variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (synonymous variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (synonymous variant) | WDR26-related disorder | |
| | | Indel (nonsense) | not provided | |
| | | Single nucleotide variant (splice donor variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (nonsense) | WDR26-related disorder | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (splice acceptor variant) | See cases | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Duplication (frameshift variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Skraban-Deardorff syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |