ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.91936A>C (p.Asn30646His)

dbSNP: rs786205328
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001723337 SCV001958415 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001723337 SCV001971071 uncertain significance not provided no assertion criteria provided clinical testing

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