ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.*1652GAATT[1]

dbSNP: rs886049224
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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 RCV000332165 SCV000377985 uncertain significance Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000370444 SCV000377986 uncertain significance Timothy syndrome 2016-06-14 criteria provided, single submitter clinical testing

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