ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.873A>G (p.Ser291=)

dbSNP: rs1848362899
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001843084 SCV001346274 likely benign Cardiac arrhythmia 2018-12-16 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006722 SCV004838794 likely benign Long QT syndrome 2023-06-26 criteria provided, single submitter clinical testing

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