| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (splice donor variant +1 more) | Meacham syndrome +6 more | GPathogenic/Likely pathogenic |
| | | Insertion (frameshift variant +2 more) | WT1-related disorder | |
| | LOC107982234, WT1 (V167D +1 more) | Single nucleotide variant (missense variant +1 more) | Nephrotic syndrome, type 4 | |
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