"Genome Diagnostics Laboratory, The Hospital for Sick Children"[submit - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 515922	NM_024426.6(WT1):c.1568G>A (p.Ter523=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +7 more	GConflicting classifications of pathogenicity
Select item 419332	NM_024426.6(WT1):c.1400G>A (p.Arg467Gln)	WT1 (R250Q +10 more)	Single nucleotide variant (missense variant +1 more)	Kidney disorder +10 more	GPathogenic/Likely pathogenic
Select item 3487	NM_024426.6(WT1):c.1399C>T (p.Arg467Trp)	WT1 (R250W +9 more)	Single nucleotide variant (missense variant +1 more)	not provided +9 more	GPathogenic/Likely pathogenic
Select item 3494	NM_024426.6(WT1):c.1387C>T (p.Arg463Ter)	WT1 (R246* +9 more)	Single nucleotide variant (nonsense +1 more)	not provided +9 more	GPathogenic
Select item 599126	NM_024426.6(WT1):c.1180C>T (p.Arg394Cys)	WT1 (R177C +8 more)	Single nucleotide variant (missense variant +2 more)	Focal segmental glomerulosclerosis +5 more	GUncertain significance
Select item 241475	NM_024426.6(WT1):c.1114-9T>C	WT1	Single nucleotide variant (intron variant)	not provided +10 more	GBenign/Likely benign
Select item 261708	NM_024426.6(WT1):c.1074A>G (p.Gln358=)	WT1	Single nucleotide variant (synonymous variant +2 more)	not specified +9 more	GBenign
Select item 261712	NM_024426.6(WT1):c.513C>A (p.Gly171=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +8 more	GBenign/Likely benign
Select item 241476	NM_024426.6(WT1):c.181C>A (p.Arg61=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Nephrotic syndrome, type 4 +9 more	GBenign/Likely benign