List of variants reported as likely pathogenic for embryonal neoplasm by All of Us Research Program, National Institutes of Health

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.965+1G>A	rs771527206	0.00001
NM_024426.6(WT1):c.1447+4C>T	rs587776577

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