ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.392+3A>G

dbSNP: rs2062503289
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals RCV001175250 SCV001338830 uncertain significance Brugada syndrome 2019-12-17 no assertion criteria provided clinical testing

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