ClinVar Miner

Submissions for variant NM_006888.6(CALM1):c.421+16C>G

dbSNP: rs267607279
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005222769 SCV005869877 likely benign Catecholaminergic polymorphic ventricular tachycardia 4; Long QT syndrome 14 2024-05-01 criteria provided, single submitter clinical testing
Nyegaard lab; Aarhus University RCV000149484 SCV000187715 benign not provided 2012-07-23 no assertion criteria provided research

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