ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as pathogenic for Wilms tumor

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_024426.6(WT1):c.334del (p.Asp112fs) rs1554946600
NM_024426.6(WT1):c.472G>T (p.Glu158Ter) rs1565001383
NM_024426.6(WT1):c.478C>T (p.Gln160Ter) rs1554946500
NM_024426.6(WT1):c.546C>A (p.Tyr182Ter) rs121907911
NM_024426.6(WT1):c.592del (p.Ala198fs) rs1131690795
NM_024426.6(WT1):c.653del (p.Arg218fs) rs1565000973

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