ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.18872C>T (p.Pro6291Leu)

dbSNP: rs2079914758
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001730305 SCV001978550 uncertain significance not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001730305 SCV001979506 uncertain significance not provided no assertion criteria provided clinical testing

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