ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.62861dup (p.Val20955fs)

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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 RCV005404829 SCV006068808 pathogenic Cardiovascular phenotype 2024-01-18 criteria provided, single submitter clinical testing PVS1, PM2, PP1

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