| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense +2 more) | Inborn genetic diseases +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Mixed Phenotype Acute Leukemia with t(v;11q23.3); KMT2A Rearranged | |
| | | Duplication (frameshift variant +1 more) | Wilms tumor 1 | |
| | | Single nucleotide variant (nonsense +1 more) | Wilms tumor 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Deletion (frameshift variant +3 more) | Wilms tumor 1 | |
| | | Microsatellite (inframe_insertion +1 more) | Drash syndrome +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Deletion (frameshift variant +1 more) | Drash syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | GConflicting classifications of pathogenicity |
| | LOC107982234, WT1 (R19G +1 more) | Single nucleotide variant (missense variant +1 more) | Wilms tumor 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Drash syndrome +4 more | |
Click to view in NCBI Gene