ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.88068G>A (p.Trp29356Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV004781985 SCV005393876 likely pathogenic Dilated cardiomyopathy 1G no assertion criteria provided clinical testing

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