List of variants in gene WT1 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.1161A>G (p.Ala387=)	rs141834493	0.00051
NM_024426.6(WT1):c.1063T>C (p.Cys355Arg)	rs142059681	0.00044
NM_024426.6(WT1):c.1182C>T (p.Arg394=)	rs147939483	0.00027
NM_024426.6(WT1):c.760C>T (p.Pro254Ser)	rs2234584	0.00022
NM_024426.6(WT1):c.1404C>T (p.Ser468=)	rs374799820	0.00006
NM_024426.6(WT1):c.696C>T (p.Ser232=)	rs9332974	0.00006
NM_024426.6(WT1):c.785G>A (p.Gly262Asp)	rs372225738	0.00006
NM_024426.6(WT1):c.1017-4G>C	rs1043846933	0.00002
NM_024426.6(WT1):c.1563G>A (p.Ala521=)	rs202118284	0.00002
NM_024426.6(WT1):c.1568G>A (p.Ter523=)	rs148856160	0.00001
NM_024426.6(WT1):c.*5T>C	rs765743928
NM_024426.6(WT1):c.1114-3C>A
NM_024426.6(WT1):c.1242G>A (p.Gln414=)
NM_024426.6(WT1):c.1448-10G>T	rs185744719
NM_024426.6(WT1):c.764T>A (p.Met255Lys)	rs377573993
NM_024426.6(WT1):c.784+7G>C	rs1033235205
NM_024426.6(WT1):c.900C>T (p.Tyr300=)	rs190440703

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