List of variants reported as likely benign for Nephrotic syndrome, type 4

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Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.*1132A>T	rs5030328	0.02340
NM_024426.6(WT1):c.*835A>G	rs5030322	0.02303
NM_024426.6(WT1):c.*1209A>G	rs5030329	0.00900
NM_024426.6(WT1):c.*1098C>T	rs5030327	0.00867
NM_024426.6(WT1):c.*897G>C	rs5030324	0.00520
NM_024426.6(WT1):c.1114-9T>C	rs5030274	0.00465
NM_024426.6(WT1):c.*16G>T	rs2234594	0.00421
NM_024426.6(WT1):c.*542G>A	rs142726499	0.00380
NM_024426.6(WT1):c.*903G>A	rs5030325	0.00370
NM_024426.6(WT1):c.181C>A (p.Arg61=)	rs2234581	0.00270
NM_024426.6(WT1):c.123G>C (p.Pro41=)	rs555140661	0.00188
NM_024426.6(WT1):c.*138G>A	rs111351882	0.00165
NM_024426.6(WT1):c.216G>T (p.Gln72His)	rs5030135	0.00036
NM_024426.6(WT1):c.760C>T (p.Pro254Ser)	rs2234584	0.00022
NM_024426.6(WT1):c.513C>A (p.Gly171=)	rs536728682	0.00004
NM_024426.6(WT1):c.1154G>A (p.Arg385Gln)	rs147241955	0.00003
NM_024426.6(WT1):c.*1239T>A	rs534396876
NM_024426.6(WT1):c.*345G>A	rs5030318
NM_024426.6(WT1):c.*864T>A	rs5030323
NM_024426.6(WT1):c.*864T>G	rs5030323

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