ClinVar Miner

Submissions for variant NM_006073.4(TRDN):c.1975+8C>T

gnomAD frequency: 0.00006  dbSNP: rs754046696
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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 RCV002562006 SCV001682394 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2025-01-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501652 SCV002806590 likely benign Catecholaminergic polymorphic ventricular tachycardia 1; Catecholaminergic polymorphic ventricular tachycardia 5 2021-08-20 criteria provided, single submitter clinical testing

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