Variants in gene WT1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.1131T>C (p.Pro377=)	rs151034312	0.00047
NM_024426.6(WT1):c.1063T>C (p.Cys355Arg)	rs142059681	0.00044
NM_024426.6(WT1):c.662-6C>A	rs372418954	0.00034
NM_024426.6(WT1):c.760C>T (p.Pro254Ser)	rs2234584	0.00022
NM_024426.6(WT1):c.785G>A (p.Gly262Asp)	rs372225738	0.00006
NM_024426.6(WT1):c.764T>A (p.Met255Lys)	rs377573993

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