ClinVar Miner

Submissions for variant NM_004456.5(EZH2):c.2111-8C>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 RCV003613518 SCV004461434 likely benign Weaver syndrome 2023-04-28 criteria provided, single submitter clinical testing

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