ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.887+20T>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003061380 SCV003459139 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-10-14 criteria provided, single submitter clinical testing

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