ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.326T>G (p.Leu109Arg)

dbSNP: rs199473498
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000988006 SCV001137552 benign Long QT syndrome 2 2019-05-28 criteria provided, single submitter clinical testing
Cardiovascular Biomedical Research Unit, Royal Brompton & Harefield NHS Foundation Trust RCV000058213 SCV000089733 not provided not provided no assertion provided literature only

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