ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.58494dup (p.Ile19499fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV005404060 SCV006065492 pathogenic Cardiovascular phenotype 2022-07-20 criteria provided, single submitter clinical testing

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