ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1329C>A (p.Leu443=)

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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 RCV003787320 SCV004576327 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-05-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004005991 SCV004839394 likely benign Wilms tumor 1 2023-11-02 criteria provided, single submitter clinical testing

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