ClinVar Miner

Submissions for variant NM_004456.5(EZH2):c.1061G>A (p.Arg354His)

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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 RCV003613398 SCV004456062 likely benign Weaver syndrome 2023-10-06 criteria provided, single submitter clinical testing

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