ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.42557C>T (p.Thr14186Ile)

dbSNP: rs369771893
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001817649 SCV002072177 uncertain significance not specified 2017-11-22 criteria provided, single submitter clinical testing

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