ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.214-61251C>A

gnomAD frequency: 0.00414  dbSNP: rs117558767
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000324332 SCV000483058 likely benign Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001683462 SCV001900011 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002504198 SCV002809249 benign Brugada syndrome 4 2022-03-15 criteria provided, single submitter clinical testing

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