ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.5140G>A (p.Val1714Ile)

dbSNP: rs1553612991
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV000624379 SCV000740411 uncertain significance Brugada syndrome 2017-06-02 criteria provided, single submitter clinical testing

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