"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "LO - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 261713	NM_024426.6(WT1):c.609C>T (p.Asn203=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	WT1-related condition +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 193454	NM_024426.6(WT1):c.345C>T (p.Pro115=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +8 more	GBenign
Select item 241480	NM_024426.6(WT1):c.309C>A (p.Gly103=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +7 more	GConflicting classifications of pathogenicity
Select item 241479	NM_024426.6(WT1):c.216G>T (p.Gln72His)	LOC107982234, WT1 (Q72H)	Single nucleotide variant (missense variant +1 more)	WT1-related condition +8 more	GBenign/Likely benign
Select item 261710	NM_024426.6(WT1):c.213G>T (p.Pro71=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +8 more	GBenign

ClinVar