ClinVar Miner

Submissions for variant NM_004456.5(EZH2):c.1890G>A (p.Gly630=)

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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 RCV005179576 SCV005815389 benign Weaver syndrome 2024-09-17 criteria provided, single submitter clinical testing

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