ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.76397T>C (p.Ile25466Thr)

dbSNP: rs780302234
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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 RCV001730340 SCV001978824 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001730340 SCV001980450 uncertain significance not provided no assertion criteria provided clinical testing

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