ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.448+77C>T

gnomAD frequency: 0.00001  dbSNP: rs2064230789
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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 RCV002073890 SCV002429899 likely benign Brugada syndrome 5 2020-11-23 criteria provided, single submitter clinical testing

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