ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.34449del (p.Val11485fs)

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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 RCV005404815 SCV006068749 uncertain significance Cardiovascular phenotype 2025-04-09 criteria provided, single submitter clinical testing

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