ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1354+14C>T

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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 RCV003780536 SCV004568346 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-10-20 criteria provided, single submitter clinical testing

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