ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.1066G>T (p.Asp356Tyr)

dbSNP: rs199473565
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV000790455 SCV000929782 likely pathogenic Brugada syndrome 1 2018-11-02 criteria provided, single submitter clinical testing

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