| | | Duplication | Wilms tumor 1 +3 more | |
| | | Duplication | Wilms tumor 1 +3 more | |
| | | Deletion | Wilms tumor 1 +3 more | |
| | | Deletion | Wilms tumor 1 +3 more | |
| | | Deletion | Wilms tumor 1 +3 more | |
| | | Deletion | Wilms tumor 1 +3 more | |
| | | Deletion | Wilms tumor 1 +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (P136L +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Deletion (nonsense +3 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | | Duplication (inframe_insertion +2 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +3 more) | Frasier syndrome +3 more | |
| | | Deletion (frameshift variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (S119L +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Indel (intron variant) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (G186D +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (L85P +1 more) | Single nucleotide variant (missense variant +1 more) | Wilms tumor 1 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Deletion (frameshift variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Deletion (frameshift variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (M195V +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (Q26E +1 more) | Single nucleotide variant (missense variant +1 more) | Wilms tumor 1 +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Drash syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Drash syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +3 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (F164S +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Deletion (frameshift variant +2 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (F108S +1 more) | Single nucleotide variant (missense variant +1 more) | Drash syndrome +3 more | |
| | LOC107982234, WT1 (D8V +1 more) | Single nucleotide variant (missense variant +1 more) | Drash syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (N219fs) | Duplication (frameshift variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (P104S +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (P17S +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (P130L +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +3 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (N77K +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (L106P +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (P33Q +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (A128E +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Duplication (intron variant) | Frasier syndrome +3 more | |
| | | Duplication (frameshift variant +1 more) | Frasier syndrome +3 more | |
| | | Deletion (frameshift variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +3 more) | Drash syndrome +3 more | |
| | LOC107982234, WT1 (G178E +1 more) | Single nucleotide variant (missense variant +1 more) | Drash syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Wilms tumor 1 +3 more | GConflicting classifications of pathogenicity |
| | LOC107982234, WT1 (N77D +1 more) | Single nucleotide variant (missense variant +1 more) | Drash syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +3 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +3 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (F113Y +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (D35A +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (S150I +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (R19S +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (L43* +1 more) | Single nucleotide variant (nonsense +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (G173R +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (R56* +1 more) | Indel (nonsense +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (C180Y +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (G32E +1 more) | Single nucleotide variant (missense variant +1 more) | Drash syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Frasier syndrome +3 more | |
| | LOC107982234, WT1 (F185V +1 more) | Single nucleotide variant (missense variant +1 more) | Frasier syndrome +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Frasier syndrome +3 more | |