ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.910T>G (p.Trp304Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory - Cardiogenetics, CHU de Nantes RCV003319960 SCV004024160 likely pathogenic Long QT syndrome 1 2023-08-01 criteria provided, single submitter clinical testing

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