ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.1090T>C (p.Phe364Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
New York Genome Center RCV003228631 SCV003925297 uncertain significance Atrial fibrillation, familial, 3; Long QT syndrome 1; Jervell and Lange-Nielsen syndrome 1; Short QT syndrome type 2 2022-08-28 criteria provided, single submitter clinical testing

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