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

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.*897G>C	rs5030324	0.00520
NM_024426.6(WT1):c.*542G>A	rs142726499	0.00380
NM_024426.6(WT1):c.*138G>A	rs111351882	0.00165
NM_024426.6(WT1):c.1161A>G (p.Ala387=)	rs141834493	0.00051
NM_024426.6(WT1):c.1264+19C>T	rs2234592	0.00010
NM_024426.6(WT1):c.849C>T (p.Thr283=)	rs145425799	0.00010
NM_024426.6(WT1):c.887+14G>A	rs757237600	0.00008
NM_024426.6(WT1):c.785G>A (p.Gly262Asp)	rs372225738	0.00006
NM_024426.6(WT1):c.1016+15C>T	rs752756426	0.00004
NM_024426.6(WT1):c.1038C>T (p.Ser346=)	rs750018485	0.00003
NM_024426.6(WT1):c.887+4G>A	rs778673400	0.00002
NM_024426.6(WT1):c.1198T>C (p.Tyr400His)	rs746353651	0.00001
NM_024426.6(WT1):c.1568G>A (p.Ter523=)	rs148856160	0.00001
NM_024426.6(WT1):c.945C>T (p.Asn315=)	rs775085343	0.00001
NM_024426.6(WT1):c.1448-10G>A	rs185744719
NM_024426.6(WT1):c.662-10G>T	rs1554945255
NM_024426.6(WT1):c.708G>A (p.Thr236=)	rs768828897
NM_024426.6(WT1):c.764T>A (p.Met255Lys)	rs377573993
NM_024426.6(WT1):c.780G>A (p.Ser260=)	rs1403311573

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