ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.5760C>T (p.Ser1920=)

gnomAD frequency: 0.00002  dbSNP: rs747009227
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002080701 SCV002380735 likely benign Brugada syndrome 2024-05-25 criteria provided, single submitter clinical testing

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