ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.684-4G>T

dbSNP: rs750965939
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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 RCV001843280 SCV001352548 likely benign Cardiac arrhythmia 2019-12-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068431 SCV002434921 likely benign Long QT syndrome 2021-06-19 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002068431 SCV004833453 likely benign Long QT syndrome 2023-07-10 criteria provided, single submitter clinical testing

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