ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.23916C>T (p.Cys7972=)

dbSNP: rs2078030706
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Academic Medical Center RCV001700892 SCV001924593 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001724405 SCV001952886 likely benign not provided no assertion criteria provided clinical testing

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