ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.1978C>T (p.Gln660Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen RCV004584257 SCV005068266 pathogenic Brugada syndrome 1 2024-07-02 criteria provided, single submitter clinical testing

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