List of variants reported as benign for embryonal neoplasm by Genome-Nilou Lab

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.*267G>C	rs5030317	0.44381
NM_024426.6(WT1):c.1448-49T>C	rs1799937	0.34839
NM_024426.6(WT1):c.213G>T (p.Pro71=)	rs2234582	0.31689
NM_024426.6(WT1):c.887+16G>A	rs1799933	0.26810
NM_024426.6(WT1):c.1122A>G (p.Arg374=)	rs16754	0.16617
NM_024426.6(WT1):c.345C>T (p.Pro115=)	rs1799925	0.15374
NM_024426.6(WT1):c.*88A>G	rs5030315	0.14706
NM_024426.6(WT1):c.*224A>G	rs5030316	0.13669
NM_024426.6(WT1):c.609C>T (p.Asn203=)	rs2234583	0.13287
NM_024426.6(WT1):c.1265-32C>A	rs2234593	0.12726
NM_024426.6(WT1):c.1074A>G (p.Gln358=)	rs2234590	0.04693
NM_024426.6(WT1):c.662-1928_662-1927del	rs71873106	0.02282
NM_024426.6(WT1):c.785-20G>T	rs5030168	0.00663
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.181C>A (p.Arg61=)	rs2234581	0.00270
NM_024426.6(WT1):c.216G>T (p.Gln72His)	rs5030135	0.00036
NM_024426.6(WT1):c.513C>A (p.Gly171=)	rs536728682	0.00004

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