"Human Genetics Disease in Children – Taif University, Taif University - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3488	NM_024426.6(WT1):c.1316G>A (p.Arg439His)	WT1 (R222H +8 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +8 more	GPathogenic
Select item 224479	NM_024426.6(WT1):c.1265-32C>A	WT1	Single nucleotide variant (intron variant)	not specified +6 more	GBenign
Select item 224480	NM_024426.6(WT1):c.1265-52G>T	WT1	Single nucleotide variant (intron variant)	Drash syndrome	GBenign

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