ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.88658T>G (p.Leu29553Arg)

dbSNP: rs1453445227
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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 RCV001700825 SCV001926174 uncertain significance not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001700825 SCV001955836 uncertain significance not provided no assertion criteria provided clinical testing

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