ClinVar Miner

Submissions for variant NM_006073.4(TRDN):c.2051-19G>A

gnomAD frequency: 0.42872  dbSNP: rs7754205
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253279 SCV000311375 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000253279 SCV000520321 benign not specified 2016-09-21 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000253279 SCV001774664 benign not specified 2021-07-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838582 SCV002098717 benign Catecholaminergic polymorphic ventricular tachycardia 5 2021-09-10 criteria provided, single submitter clinical testing
Invitae RCV002518636 SCV002464255 benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-02-01 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000253279 SCV001922148 benign not specified no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000253279 SCV001963568 benign not specified no assertion criteria provided clinical testing

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