ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.63185T>C (p.Ile21062Thr)

dbSNP: rs575313522
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194509 SCV000249273 uncertain significance not specified 2015-07-17 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV004791318 SCV005413065 uncertain significance not provided 2024-09-09 criteria provided, single submitter clinical testing

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