ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.4201_4203del (p.Phe1401del)

dbSNP: rs1559414131
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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 RCV000678916 SCV000805121 likely pathogenic Brugada syndrome 2017-11-16 criteria provided, single submitter clinical testing

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