ClinVar Miner

List of variants in gene WT1 reported as likely benign by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 26
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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.*1209A>G rs5030329 0.00900
NM_024426.6(WT1):c.*1098C>T rs5030327 0.00867
NM_024426.6(WT1):c.*897G>C rs5030324 0.00520
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.*542G>A rs142726499 0.00380
NM_024426.6(WT1):c.*903G>A rs5030325 0.00370
NM_024426.6(WT1):c.*138G>A rs111351882 0.00165
NM_024426.6(WT1):c.1131T>C (p.Pro377=) rs151034312 0.00047
NM_024426.6(WT1):c.*12C>T rs77462662 0.00034
NM_024426.6(WT1):c.760C>T (p.Pro254Ser) rs2234584 0.00022
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.1124G>A (p.Arg375His) rs554416372 0.00003
NM_024426.6(WT1):c.1154G>A (p.Arg385Gln) rs147241955 0.00003
NM_024426.6(WT1):c.887+4G>A rs778673400 0.00002
NM_024426.6(WT1):c.1198T>C (p.Tyr400His) rs746353651 0.00001
NM_024426.6(WT1):c.1568G>A (p.Ter523=) rs148856160 0.00001
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.695G>C (p.Ser232Thr) rs761913397

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