ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.23616C>T (p.Asn7872=) (rs181206334)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000082373 SCV000114350 uncertain significance not provided 2013-10-28 criteria provided, single submitter clinical testing
Invitae RCV001086234 SCV000642839 likely benign Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2020-07-08 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000082373 SCV001153038 likely benign not provided 2018-10-01 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001582572 SCV001821414 likely benign not specified 2021-08-28 criteria provided, single submitter clinical testing
GeneDx RCV000082373 SCV001838892 likely benign not provided 2021-04-01 criteria provided, single submitter clinical testing

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