ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.65655del (p.Thr21886fs)

dbSNP: rs1575948935
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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 RCV000845376 SCV000987434 likely pathogenic Primary familial dilated cardiomyopathy criteria provided, single submitter clinical testing

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