ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.6780+27G>A

gnomAD frequency: 0.00029  dbSNP: rs16053
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
GeneDx RCV001648570 SCV001861568 benign not provided 2020-07-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001648570 SCV005314805 benign not provided criteria provided, single submitter not provided

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