ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.*5421del

dbSNP: rs10713809
Minimum review status: Collection method:
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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 RCV000287349 SCV000378119 benign Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000342355 SCV000378120 benign Timothy syndrome 2016-06-14 criteria provided, single submitter clinical testing

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