ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.*835AAGT[3]

dbSNP: rs547804393
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000266499 SCV000361857 uncertain significance Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003417967 SCV004126528 benign not provided 2022-09-01 criteria provided, single submitter clinical testing CACNB2: BS1, BS2

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