ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.714C>A (p.Thr238=)

dbSNP: rs769388483
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001718935 SCV000721869 likely benign not provided 2018-04-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001718935 SCV003296519 likely benign not provided 2022-08-15 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003591759 SCV004362233 likely benign Cardiac arrhythmia 2023-04-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV003591759 SCV004824185 likely benign Cardiac arrhythmia 2023-07-10 criteria provided, single submitter clinical testing

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