ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.67302T>G (p.Tyr22434Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, University of Leuven RCV003237368 SCV002817398 likely pathogenic Primary dilated cardiomyopathy 2022-12-31 criteria provided, single submitter clinical testing

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