ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.867C>T (p.Tyr289=)

gnomAD frequency: 0.00001  dbSNP: rs1163235946
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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 RCV002132570 SCV002432146 likely benign Brugada syndrome 2021-11-04 criteria provided, single submitter clinical testing

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