Variants in gene WT1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.1348C>T (p.His450Tyr)	rs28942089
NM_024426.6(WT1):c.1388G>A (p.Arg463Gln)	rs1037084691
NM_024426.6(WT1):c.1400G>A (p.Arg467Gln)	rs121907903
NM_024426.6(WT1):c.1447+4C>T	rs587776577

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