ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.1413C>T (p.Ser471=)

gnomAD frequency: 0.00001  dbSNP: rs780041998
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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 RCV001843058 SCV001345041 likely benign Cardiac arrhythmia 2019-02-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003657047 SCV001672250 likely benign not provided 2024-08-16 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001843058 SCV004819651 likely benign Cardiac arrhythmia 2024-03-24 criteria provided, single submitter clinical testing

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