List of variants in gene WT1 reported as likely benign for not provided

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.*1132A>T	rs5030328	0.02340
NM_024426.6(WT1):c.*835A>G	rs5030322	0.02303
NM_024426.6(WT1):c.1265-249C>T	rs113403661	0.01542
NM_024426.6(WT1):c.1114-160G>A	rs73473740	0.01502
NM_024426.6(WT1):c.888-98G>A	rs5030196	0.01071
NM_024426.6(WT1):c.785-172A>C	rs144615463	0.01005
NM_024426.6(WT1):c.1016+81C>T	rs5030208	0.00829
NM_024426.6(WT1):c.1265-173C>T	rs149529057	0.00822
NM_024426.6(WT1):c.1355-87G>A	rs5030290	0.00796
NM_024426.6(WT1):c.1265-141T>G	rs5030288	0.00768
NM_024426.6(WT1):c.662-211G>C	rs5030164	0.00737
NM_024426.6(WT1):c.887+229G>A	rs5030173	0.00617
NM_024426.6(WT1):c.1114-9T>C	rs5030274	0.00465
NM_024426.6(WT1):c.*16G>T	rs2234594	0.00421
NM_024426.6(WT1):c.785-160T>C	rs186598490	0.00116
NM_024426.6(WT1):c.1131T>C (p.Pro377=)	rs151034312	0.00047
NM_024426.6(WT1):c.662-6C>A	rs372418954	0.00034
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.1146T>A (p.Thr382=)	rs371168589	0.00006
NM_024426.6(WT1):c.1404C>T (p.Ser468=)	rs374799820	0.00006
NM_024426.6(WT1):c.1568G>A (p.Ter523=)	rs148856160	0.00001
NM_024426.6(WT1):c.662-5C>T	rs780259089	0.00001
NM_024426.6(WT1):c.1032C>T (p.Tyr344=)	rs1338914258
NM_024426.6(WT1):c.1265-218del	rs111384963
NM_024426.6(WT1):c.1448-10G>T	rs185744719
NM_024426.6(WT1):c.662-80del	rs34924443
NM_024426.6(WT1):c.785-14G>C	rs375514482
NM_024426.6(WT1):c.900C>T (p.Tyr300=)	rs190440703
NR_023920.1(WT1-AS):n.1514C>T
NR_023920.2(WT1-AS):n.791T>C

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