ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.1206+6T>C

gnomAD frequency: 0.00575  dbSNP: rs147857449
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000463017 SCV000562843 benign Brugada syndrome 4 2025-01-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000463017 SCV001472335 benign Brugada syndrome 4 2020-10-20 criteria provided, single submitter clinical testing
GeneDx RCV001672428 SCV001891867 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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