ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.1911C>T (p.His637=)

dbSNP: rs2134097230
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001842123 SCV001735559 likely benign Cardiac arrhythmia 2020-12-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003533006 SCV004273283 likely benign Long QT syndrome 2024-07-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV003533006 SCV005426396 likely benign Long QT syndrome 2024-07-20 criteria provided, single submitter clinical testing

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