ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.76670T>C (p.Ile25557Thr)

dbSNP: rs758441370
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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 RCV005404196 SCV006069980 likely benign not specified 2025-04-09 criteria provided, single submitter clinical testing

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