ClinVar Miner

Submissions for variant NM_006073.4(TRDN):c.610+19A>G

gnomAD frequency: 0.00001  dbSNP: rs1482036297
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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 RCV003033315 SCV002417849 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-01-17 criteria provided, single submitter clinical testing

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