ClinVar Miner

List of variants reported as likely benign for Wilms tumor by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_024426.6(WT1):c.*1098C>T rs5030327
NM_024426.6(WT1):c.*1132A>T rs5030328
NM_024426.6(WT1):c.*1209A>G rs5030329
NM_024426.6(WT1):c.*1239T>A rs534396876
NM_024426.6(WT1):c.*138G>A rs111351882
NM_024426.6(WT1):c.*16G>T rs2234594
NM_024426.6(WT1):c.*224A>G rs5030316
NM_024426.6(WT1):c.*345G>A rs5030318
NM_024426.6(WT1):c.*542G>A rs142726499
NM_024426.6(WT1):c.*820G>C rs1042347
NM_024426.6(WT1):c.*835A>G rs5030322
NM_024426.6(WT1):c.*864T>A rs5030323
NM_024426.6(WT1):c.*864T>G rs5030323
NM_024426.6(WT1):c.*88A>G rs5030315
NM_024426.6(WT1):c.*897G>C rs5030324
NM_024426.6(WT1):c.*903G>A rs5030325
NM_024426.6(WT1):c.1074A>G (p.Gln358=) rs2234590
NM_024426.6(WT1):c.1114-9T>C rs5030274
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661
NM_024426.6(WT1):c.181C>A (p.Arg61=) rs2234581
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682
NM_024426.6(WT1):c.609C>T (p.Asn203=) rs2234583
NM_024426.6(WT1):c.696C>T (p.Ser232=) rs9332974

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