ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.*652_*659GCC[2]GGGAAGGGGCCGCCGG[1]

dbSNP: rs71057834
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000394635 SCV000377955 benign Timothy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000311296 SCV000377956 benign Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing

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