List of variants in gene WT1 reported as uncertain significance for Nephroblastoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.*574del	rs5030319	0.00007
NM_024426.6(WT1):c.*1021GT[14]	rs58549495
NM_024426.6(WT1):c.*1021GT[15]	rs58549495
NM_024426.6(WT1):c.*1021GT[18]	rs58549495
NM_024426.6(WT1):c.*1021GT[19]	rs58549495
NM_024426.6(WT1):c.*1021GT[20]	rs58549495
NM_024426.6(WT1):c.*1058G>T	rs886048211
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.*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.*841C>A	rs886048213

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