List of variants in gene WT1 reported as benign for syndrome caused by partial chromosomal deletion

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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: 20

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.887+16G>A	rs1799933	0.26810
NM_024426.6(WT1):c.1122A>G (p.Arg374=)	rs16754	0.16617
NC_000011.10:g.32438918G>A	rs6508	0.16158
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.1161A>G (p.Ala387=)	rs141834493	0.00051
NM_024426.6(WT1):c.1131T>C (p.Pro377=)	rs151034312	0.00047
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.887+14G>A	rs757237600	0.00008
NM_024426.6(WT1):c.1017-9T>C	rs368486676	0.00007
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.965+14T>C	rs369920807	0.00004
NM_024426.6(WT1):c.1017-20dup
NM_024426.6(WT1):c.1122A>C (p.Arg374=)	rs16754
NM_024426.6(WT1):c.1448-10G>A	rs185744719
NM_024426.6(WT1):c.695G>C (p.Ser232Thr)	rs761913397
NM_024426.6(WT1):c.888-8dup

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