ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.1207-7T>C

dbSNP: rs1589754337
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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 RCV001470703 SCV001674801 likely benign Brugada syndrome 4 2018-11-30 criteria provided, single submitter clinical testing

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