ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.1827del (p.Glu610fs)

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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 RCV004771818 SCV005382574 likely pathogenic Brugada syndrome 2024-02-09 no assertion criteria provided clinical testing

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