ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.120+379A>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003622412 SCV004562368 benign Brugada syndrome 4 2023-10-26 criteria provided, single submitter clinical testing

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