| | | Single nucleotide variant (nonsense +2 more) | Drash syndrome +3 more | |
| | WT1, LOC107982234 (A50T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +8 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +7 more | |
| | | Single nucleotide variant (intron variant) | Drash syndrome +7 more | |
| | | Single nucleotide variant (intron variant) | Drash syndrome +7 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Meacham syndrome +7 more | |
| | | Single nucleotide variant (intron variant) | Wilms tumor 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Wilms tumor 1 +7 more | |
| | | Single nucleotide variant (intron variant) | Wilms tumor 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Wilms tumor 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +7 more | |
| | | Single nucleotide variant (missense variant +2 more) | Aniridia 1 +7 more | |
| | | Single nucleotide variant (missense variant +2 more) | Aniridia 1 +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Aniridia 1 +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Aniridia 1 +7 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mesothelioma, malignant +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Mesothelioma, malignant +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Drash syndrome +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | Aniridia 1 +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Nephrotic syndrome, type 4 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Nephrotic syndrome, type 4 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Nephrotic syndrome, type 4 +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | Wilms tumor 1 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Wilms tumor 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Nephrotic syndrome, type 4 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Wilms tumor 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Wilms tumor 1 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Nephrotic syndrome, type 4 +2 more | |
| | | Single nucleotide variant (synonymous variant +3 more) | Wilms tumor 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Drash syndrome +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Drash syndrome +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Meacham syndrome +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Nephrotic syndrome, type 4 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | WT1-related disorder +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Wilms tumor 1 +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Drash syndrome +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Drash syndrome +7 more | |
| | | Single nucleotide variant (missense variant +2 more) | Aniridia 1 +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Wilms tumor 1 +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Wilms tumor 1 +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Aniridia 1 +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Aniridia 1 +8 more | |
| | | Single nucleotide variant (synonymous variant +3 more) | Frasier syndrome +7 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Frasier syndrome +7 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +7 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +7 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Inborn genetic diseases +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Wilms tumor 1 +7 more | |
| | | Indel (missense variant +1 more) | Wilms tumor 1 +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | Drash syndrome +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | WT1-related disorder +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Wilms tumor 1 +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Wilms tumor 1 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Aniridia 1 +10 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | WT1-related disorder +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | WT1-related disorder +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +7 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | WT1-related disorder +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Nephrotic syndrome, type 4 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Aniridia 1 +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +9 more | |
| | | Single nucleotide variant (missense variant +2 more) | Wilms tumor 1 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Nephrotic syndrome, type 4 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Drash syndrome +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Meacham syndrome +8 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Meacham syndrome +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Meacham syndrome +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Meacham syndrome +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Drash syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Meacham syndrome +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Meacham syndrome +4 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Nephrotic syndrome, type 4 +3 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | 11p partial monosomy syndrome +3 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | 11p partial monosomy syndrome +3 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Meacham syndrome +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | 11p partial monosomy syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | 11p partial monosomy syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Meacham syndrome +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Meacham syndrome +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | 11p partial monosomy syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | 11p partial monosomy syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Meacham syndrome +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Meacham syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Nephrotic syndrome, type 4 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Meacham syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Meacham syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Meacham syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Meacham syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Nephroblastoma +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Meacham syndrome +5 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Wilms tumor 1 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Wilms tumor 1 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Nephroblastoma +3 more | |