ClinVar Miner

List of variants in gene WT1 reported as likely benign for Meacham syndrome

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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NM_024426.6(WT1):c.*138G>A rs111351882
NM_024426.6(WT1):c.*542G>A rs142726499
NM_024426.6(WT1):c.*897G>C rs5030324
NM_024426.6(WT1):c.1198T>C (p.Tyr400His) rs746353651
NM_024426.6(WT1):c.1568G>A (p.Ter523=) rs148856160
NM_024426.6(WT1):c.785G>A (p.Gly262Asp) rs372225738
NM_024426.6(WT1):c.887+4G>A rs778673400

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