ClinVar Miner

Submissions for variant NM_004456.5(EZH2):c.952A>G (p.Thr318Ala)

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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 RCV002908171 SCV003250361 likely benign Weaver syndrome 2022-05-04 criteria provided, single submitter clinical testing

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