ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.2486_2491del (p.Gly829_Tyr830del)

dbSNP: rs2154351525
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573236 SCV001798792 uncertain significance not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001573236 SCV001958045 uncertain significance not provided no assertion criteria provided clinical testing

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