ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.1083-68_1083-67del

dbSNP: rs146977188
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001719317 SCV001948106 benign not provided 2019-08-10 criteria provided, single submitter clinical testing

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