ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.2584G>A (p.Ala862Thr)

dbSNP: rs1283974516
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
CeGaT Center for Human Genetics Tuebingen RCV000996791 SCV001151716 uncertain significance not provided 2019-02-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000996791 SCV005192622 uncertain significance not provided criteria provided, single submitter not provided

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