ClinVar Miner

Submissions for variant NM_000219.6(KCNE1):c.292C>A (p.Arg98=)

dbSNP: rs199473362
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001394488 SCV001596174 likely benign Long QT syndrome 2020-03-11 criteria provided, single submitter clinical testing
Roden Lab, Vanderbilt University Medical Center RCV004779116 SCV005393664 not provided Long QT syndrome 5 no assertion provided in vitro

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