ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.5712C>T (p.Ala1904=)

dbSNP: rs1553692524
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003654442 SCV000637188 likely benign not provided 2017-04-26 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001841478 SCV001339895 likely benign Cardiac arrhythmia 2019-07-02 criteria provided, single submitter clinical testing

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