ClinVar Miner

Submissions for variant NM_001232.4(CASQ2):c.828G>A (p.Lys276=)

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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 RCV003639410 SCV004382394 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2023-10-15 criteria provided, single submitter clinical testing

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