ClinVar Miner

Submissions for variant NM_001160161.1(SCN5A):c.3228+1526G>A (rs199473193)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001087953 SCV001049848 likely benign Brugada syndrome 2020-02-25 criteria provided, single submitter clinical testing
Mendelics RCV000987210 SCV001136459 uncertain significance Brugada syndrome 1 2019-05-28 criteria provided, single submitter clinical testing
Cardiovascular Biomedical Research Unit,Royal Brompton & Harefield NHS Foundation Trust RCV000058564 SCV000090084 not provided not provided no assertion provided literature only This variant has been reported in the following publications (PMID:19841300;PMID:16453024;PMID:20129283).

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