ClinVar Miner

Submissions for variant NM_006888.6(CALM1):c.421+8_421+9del

gnomAD frequency: 0.00001  dbSNP: rs767443947
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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 RCV002093230 SCV002376556 likely benign Catecholaminergic polymorphic ventricular tachycardia 4; Long QT syndrome 14 2025-01-30 criteria provided, single submitter clinical testing

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