ClinVar Miner

List of variants in gene WT1 reported as uncertain significance for Meacham syndrome

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_024426.6(WT1):c.*100A>G
NM_024426.6(WT1):c.*1021_*1022GT[14] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[15] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[18] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[19] rs58549495
NM_024426.6(WT1):c.*1021_*1022GT[20] rs58549495
NM_024426.6(WT1):c.*1058G>T rs886048211
NM_024426.6(WT1):c.*1066T>G
NM_024426.6(WT1):c.*110C>T rs757474299
NM_024426.6(WT1):c.*1167T>G rs771770230
NM_024426.6(WT1):c.*1225T>C rs886048210
NM_024426.6(WT1):c.*159G>C rs746218880
NM_024426.6(WT1):c.*239G>A rs886048226
NM_024426.6(WT1):c.*269G>T rs886048225
NM_024426.6(WT1):c.*354G>T rs886048224
NM_024426.6(WT1):c.*366C>A rs886048223
NM_024426.6(WT1):c.*393G>T rs886048222
NM_024426.6(WT1):c.*460C>A rs886048221
NM_024426.6(WT1):c.*513C>T rs575602262
NM_024426.6(WT1):c.*534C>T rs868546165
NM_024426.6(WT1):c.*574del rs5030319
NM_024426.6(WT1):c.*5T>C
NM_024426.6(WT1):c.*611C>T rs886048220
NM_024426.6(WT1):c.*614A>C rs886048219
NM_024426.6(WT1):c.*629T>C
NM_024426.6(WT1):c.*666A>G rs374306749
NM_024426.6(WT1):c.*685G>T rs886048218
NM_024426.6(WT1):c.*707C>A rs886048217
NM_024426.6(WT1):c.*741G>T rs886048216
NM_024426.6(WT1):c.*768A>C rs886048215
NM_024426.6(WT1):c.*785C>A rs886048214
NM_024426.6(WT1):c.*841C>A rs886048213
NM_024426.6(WT1):c.1017-15T>C rs374441355
NM_024426.6(WT1):c.1200C>T (p.Tyr400=) rs886048227
NM_024426.6(WT1):c.813G>C (p.Pro271=)
NM_024426.6(WT1):c.973G>A (p.Ala325Thr)

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