ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.52334_52335del (p.Val17445fs)

dbSNP: rs2055522786
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, University of Leuven RCV003237359 SCV002817391 likely pathogenic Primary dilated cardiomyopathy 2022-12-31 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001730342 SCV001978841 likely pathogenic not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001730342 SCV001979468 likely pathogenic not provided no assertion criteria provided clinical testing

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