ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.30683-17_30683-8dup

dbSNP: rs368277751
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000499371 SCV000597664 likely benign not specified 2016-09-02 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001796082 SCV002036178 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001796082 SCV002038009 likely benign not provided no assertion criteria provided clinical testing

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