ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.432C>T (p.Phe144=)

gnomAD frequency: 0.00003  dbSNP: rs754173303
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000876366 SCV001018930 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-11-03 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004003113 SCV004824929 likely benign Wilms tumor 1 2023-12-18 criteria provided, single submitter clinical testing

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