ClinVar Miner

Submissions for variant NM_006514.3(SCN10A):c.1534C>G (p.Arg512Gly) (rs200714519)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues RCV000496453 SCV000588145 uncertain significance Brugada syndrome 2017-02-14 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute RCV000622755 SCV000740412 uncertain significance not specified 2017-07-26 criteria provided, single submitter clinical testing

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