ClinVar Miner

Submissions for variant NM_006073.4(TRDN):c.425-11dup

dbSNP: rs950851610
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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 RCV003154032 SCV001598740 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2023-12-27 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001803303 SCV002048143 likely benign Catecholaminergic polymorphic ventricular tachycardia 5 2020-10-04 criteria provided, single submitter clinical testing

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