ClinVar Miner

Submissions for variant NM_006073.4(TRDN):c.1721-4A>T

dbSNP: rs60743141
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002547008 SCV001538406 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-01-09 criteria provided, single submitter clinical testing
GeneDx RCV001664841 SCV001872985 likely benign not provided 2021-03-03 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003741256 SCV004564617 likely benign Catecholaminergic polymorphic ventricular tachycardia 5 2023-11-27 criteria provided, single submitter clinical testing

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