List of variants in gene combination LOC107982234, WT1 reported as likely pathogenic for embryonal neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.410del (p.Pro137fs)
NM_024426.6(WT1):c.455del (p.Gly152fs)	rs2133103216
NM_024426.6(WT1):c.512G>T (p.Gly171Val)	rs1554946480
NM_024426.6(WT1):c.649A>G (p.Ile217Val)	rs1384974578

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