ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.15A>G (p.Leu5=)

gnomAD frequency: 0.00001  dbSNP: rs747382316
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001841897 SCV000907133 likely benign Cardiac arrhythmia 2018-07-02 criteria provided, single submitter clinical testing

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