ClinVar Miner

Submissions for variant NM_181798.1(KCNQ1):c.86T>C (p.Leu29Pro)

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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 RCV000845331 SCV000987377 likely pathogenic not provided criteria provided, single submitter clinical testing

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