ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.*608_*609delinsAT

dbSNP: rs886046899
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000292032 SCV000361846 uncertain significance Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing

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