ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.26468C>T (p.Thr8823Met) (rs368151971)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000040051 SCV000063742 likely benign not specified 2015-04-03 criteria provided, single submitter clinical testing proposed classification - variant undergoing re-assessment, contact laboratory
Ambry Genetics RCV000249193 SCV000317957 uncertain significance Cardiovascular phenotype 2013-01-13 criteria provided, single submitter clinical testing There is insufficient or conflicting evidence for classification of this alteration.
GeneDx RCV001697103 SCV000722265 likely benign not provided 2020-07-31 criteria provided, single submitter clinical testing
Invitae RCV000643107 SCV000764794 uncertain significance Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2018-01-02 criteria provided, single submitter clinical testing

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