ClinVar Miner

Submissions for variant NM_006073.4(TRDN):c.931+19C>T

gnomAD frequency: 0.00003  dbSNP: rs1319851680
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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 RCV002561615 SCV002354142 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2021-12-27 criteria provided, single submitter clinical testing

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