ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.1653G>T (p.Ala551=)

dbSNP: rs397517952
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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 RCV001841927 SCV000907879 likely benign Cardiac arrhythmia 2018-10-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003657986 SCV003006911 likely benign not provided 2022-08-23 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001841927 SCV004820447 likely benign Cardiac arrhythmia 2023-03-23 criteria provided, single submitter clinical testing

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