List of variants in gene WT1 reported as benign for embryonal neoplasm

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: 39

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.*602A>G	rs5030320	0.45163
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
NC_000011.10:g.32438918G>A	rs6508	0.16158
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.*820G>C	rs1042347	0.03223
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.*1209A>G	rs5030329	0.00900
NM_024426.6(WT1):c.*1098C>T	rs5030327	0.00867
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
NM_024426.6(WT1):c.*903G>A	rs5030325	0.00370
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.*1049del	rs568803808
NM_024426.6(WT1):c.*1239T>A	rs534396876
NM_024426.6(WT1):c.*345G>A	rs5030318
NM_024426.6(WT1):c.*864T>A	rs5030323
NM_024426.6(WT1):c.*864T>G	rs5030323
NM_024426.6(WT1):c.*978dup	rs5030326
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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