ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.1372del (p.Arg458fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics and Genomics, Karolinska University Hospital RCV005087562 SCV005725429 likely pathogenic Brugada syndrome 1 2024-12-17 criteria provided, single submitter clinical testing

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