List of variants in gene WT1 reported by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.1063T>C (p.Cys355Arg)	rs142059681	0.00044
NM_024426.6(WT1):c.662-6C>A	rs372418954	0.00034
NM_024426.6(WT1):c.1017-19C>T	rs1398407708	0.00001
NM_024426.6(WT1):c.1120C>T (p.Arg374Ter)	rs1423753702	0.00001
NM_024426.6(WT1):c.662G>A (p.Gly221Asp)	rs369444006	0.00001
NM_024426.6(WT1):c.1354+4_1354+11del	rs1590332435
NM_024426.6(WT1):c.1399C>T (p.Arg467Trp)	rs121907900
NM_024426.6(WT1):c.1478G>A (p.Ser493Asn)	rs763551837
NM_024426.6(WT1):c.1541A>G (p.Asn514Ser)	rs1554938531
NM_024426.6(WT1):c.784+6C>T	rs1455790542

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