List of variants in gene combination LOC107982234, WT1 reported as uncertain significance for Nephroblastoma

Minimum submission review status:		Collection method:
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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.-31G>T	rs886048234
NM_024426.6(WT1):c.-82A>C	rs886048236
NM_024426.6(WT1):c.-86T>C	rs886048237
NM_024426.6(WT1):c.-90T>C	rs886048238
NM_024426.6(WT1):c.-94G>C	rs886048239
NM_024426.6(WT1):c.136G>T (p.Ala46Ser)	rs886048233
NM_024426.6(WT1):c.247G>T (p.Ala83Ser)	rs886048231
NM_024426.6(WT1):c.285C>T (p.Gly95=)	rs886048230
NM_024426.6(WT1):c.411GCC[5] (p.Pro141dup)	rs760304811

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