ClinVar Miner

List of variants reported as likely pathogenic for Denys-Drash syndrome

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.965+1G>A rs771527206 0.00001
NM_024426.6(WT1):c.1016+1G>A rs2133032244
NM_024426.6(WT1):c.1016+2T>G rs1852674417
NM_024426.6(WT1):c.1114-1G>T rs1851976798
NM_024426.6(WT1):c.1297T>G (p.Cys433Gly) rs121907905
NM_024426.6(WT1):c.1348C>T (p.His450Tyr) rs28942089
NM_024426.6(WT1):c.1354+4_1354+11del rs1590332435
NM_024426.6(WT1):c.1384C>T (p.Gln462Ter)
NM_024426.6(WT1):c.1405G>T (p.Asp469Tyr) rs28941778
NM_024426.6(WT1):c.1406A>G (p.Asp469Gly) rs121907902
NM_024426.6(WT1):c.1421A>C (p.His474Pro) rs1564969626
NM_024426.6(WT1):c.1447+2T>C rs1851829439
NM_024426.6(WT1):c.512G>T (p.Gly171Val) rs1554946480
NM_024426.6(WT1):c.523G>T (p.Gly175Cys) rs1590409377
NM_024426.6(WT1):c.965+2T>C

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