ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.619C>T (p.Leu207=)

gnomAD frequency: 0.00001  dbSNP: rs1060504180
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000471124 SCV000557457 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2024-12-02 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004002129 SCV004831320 likely benign Wilms tumor 1 2023-12-01 criteria provided, single submitter clinical testing

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