List of variants in gene WT1 reported as benign for Frasier syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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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.887+16G>A	rs1799933	0.26810
NM_024426.6(WT1):c.1122A>G (p.Arg374=)	rs16754	0.16617
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.1074A>G (p.Gln358=)	rs2234590	0.04693
NM_024426.6(WT1):c.785-20G>T	rs5030168	0.00663
NM_024426.6(WT1):c.1114-9T>C	rs5030274	0.00465
NM_024426.6(WT1):c.*16G>T	rs2234594	0.00421

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