ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.2941A>C (p.Met981Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MVZ Medizinische Genetik Mainz RCV003984948 SCV004801063 uncertain significance Catecholaminergic polymorphic ventricular tachycardia 1 2022-06-01 criteria provided, single submitter clinical testing PM2_SUP, PP2, BP4 (ACMG Version 3)

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