ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.7436C>G (p.Ala2479Gly)

dbSNP: rs758817759
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
Athena Diagnostics RCV000710983 SCV000841299 uncertain significance not provided 2017-09-18 criteria provided, single submitter clinical testing

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