| | | Duplication (frameshift variant) | Wiskott-Aldrich syndrome +2 more | |
| | | Single nucleotide variant (nonsense) | Thrombocytopenia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Wiskott-Aldrich syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | X-linked severe congenital neutropenia +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion (frameshift variant) | Wiskott-Aldrich syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | WAS-related condition +3 more | |
| | | Single nucleotide variant (missense variant) | Wiskott-Aldrich syndrome | |
| | | Single nucleotide variant (missense variant) | Wiskott-Aldrich syndrome +3 more | |
| | | Duplication (intron variant) | X-linked severe congenital neutropenia +4 more | |
| | | Single nucleotide variant (intron variant) | X-linked severe congenital neutropenia +3 more | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (nonsense) | Wiskott-Aldrich syndrome | |
| | | Single nucleotide variant (nonsense) | Wiskott-Aldrich syndrome | |
| | | Single nucleotide variant (splice donor variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Thrombocytopenia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Thrombocytopenia 1 | |
| | | Microsatellite | Wiskott-Aldrich syndrome | |
| | | Single nucleotide variant (missense variant) | WAS-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Wiskott-Aldrich syndrome | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Duplication (frameshift variant) | Wiskott-Aldrich syndrome | |
| | | Single nucleotide variant (splice donor variant) | Wiskott-Aldrich syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion (frameshift variant) | Wiskott-Aldrich syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | X-linked severe congenital neutropenia +3 more | |
| | | Deletion (frameshift variant) | X-linked severe congenital neutropenia +2 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (inframe_deletion) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Duplication (frameshift variant) | Thrombocytopenia 1 +2 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (nonsense) | not provided | |