ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.659-3del

dbSNP: rs370103843
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
Invitae RCV000472891 SCV000562246 benign not provided 2018-07-02 criteria provided, single submitter clinical testing
GeneDx RCV000472891 SCV001845925 benign not provided 2019-08-16 criteria provided, single submitter clinical testing

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