List of variants in gene WT1 reported as 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: 28

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.*267G>C	rs5030317	0.44381
NM_024426.6(WT1):c.1448-49T>C	rs1799937	0.34839
NM_024426.6(WT1):c.965+85A>G	rs2295081	0.33674
NM_024426.6(WT1):c.1016+122A>C	rs2234587	0.31951
NM_024426.6(WT1):c.887+228C>G	rs5030172	0.31567
NM_024426.6(WT1):c.887+16G>A	rs1799933	0.26810
NM_024426.6(WT1):c.785-195C>A	rs5030166	0.26115
NM_024426.6(WT1):c.785-57C>T	rs2234585	0.19805
NM_024426.6(WT1):c.887+85G>C	rs5030171	0.19730
NM_024426.6(WT1):c.887+82G>T	rs5030170	0.19727
NM_024426.6(WT1):c.1264+277T>G	rs5030278	0.19714
NM_024426.6(WT1):c.1122A>G (p.Arg374=)	rs16754	0.16617
NM_024426.6(WT1):c.1264+134T>A	rs5030277	0.15390
NM_024426.6(WT1):c.*88A>G	rs5030315	0.14706
NM_024426.6(WT1):c.*224A>G	rs5030316	0.13669
NM_024426.6(WT1):c.1265-32C>A	rs2234593	0.12726
NM_024426.6(WT1):c.1016+134C>T	rs2234588	0.09869
NM_024426.6(WT1):c.1016+164A>T	rs2234589	0.05411
NM_024426.6(WT1):c.1074A>G (p.Gln358=)	rs2234590	0.04693
NM_024426.6(WT1):c.1016+195T>G	rs5030212	0.04688
NM_024426.6(WT1):c.965+122A>G	rs5030198	0.04687
NM_024426.6(WT1):c.1114-9T>C	rs5030274	0.00465
NM_024426.6(WT1):c.*534C>T	rs868546165	0.00019
NC_000011.10:g.32366241A>G	rs192608967
NM_024426.6(WT1):c.1113+221G>A	rs5030262
NM_024426.6(WT1):c.1265-218dup	rs111384963
NM_024426.6(WT1):c.662-80dup	rs34924443
NR_023920.2(WT1-AS):n.343G>A

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