ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.444C>T (p.Asp148=)

dbSNP: rs2151746505
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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 RCV001398287 SCV001600055 likely benign Brugada syndrome 5 2020-10-08 criteria provided, single submitter clinical testing

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