List of variants in gene combination LOC107982234, WT1 reported as pathogenic for Wilms tumor 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.472G>T (p.Glu158Ter)	rs1565001383
NM_024426.6(WT1):c.514del (p.Gln172fs)	rs2133102575
NM_024426.6(WT1):c.546C>A (p.Tyr182Ter)	rs121907911
NM_024426.6(WT1):c.592del (p.Ala198fs)	rs1131690795

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