List of variants in gene combination LOC107982234, WT1 reported by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.124G>A (p.Gly42Ser)	rs762288656	0.00019
NM_024426.6(WT1):c.70C>T (p.Arg24Cys)	rs878855086	0.00004
NM_024426.6(WT1):c.151del (p.Ala51fs)	rs776155094	0.00003
NM_024426.6(WT1):c.154G>A (p.Glu52Lys)	rs1212035248	0.00001
NM_024426.6(WT1):c.411GCC[5] (p.Pro141dup)	rs760304811
NM_024426.6(WT1):c.70C>G (p.Arg24Gly)

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