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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WT1
(R218Q +9 more)
Single nucleotide variant
(missense variant +1 more)
Wilms tumor 1
+3 more
GUncertain significance
WT1
(R168Q +8 more)
Single nucleotide variant
(missense variant +2 more)
Meacham syndrome
+6 more
GConflicting classifications of pathogenicity
WT1
(H147Q +8 more)
Single nucleotide variant
(missense variant +2 more)
Aniridia 1
+7 more
GUncertain significance
WT1
(C138R +7 more)
Single nucleotide variant
(missense variant +2 more)
Wilms tumor 1
+6 more
GConflicting classifications of pathogenicity
WT1
(P37S +1 more)
Single nucleotide variant
(missense variant +1 more)
Nephrotic syndrome, type 4
+11 more
GConflicting classifications of pathogenicity
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