ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.27737G>T (p.Arg9246Ile)

dbSNP: rs1404441295
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Total submissions: 3
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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) RCV001573819 SCV001800223 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001573819 SCV001922613 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001573819 SCV001964168 uncertain significance not provided no assertion criteria provided clinical testing

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