ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.2142C>G (p.Asp714Glu)

dbSNP: rs121908218
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
UniProtKB/Swiss-Prot RCV000059293 SCV000090845 not provided Migraine, familial hemiplegic, 1 no assertion provided not provided
GeneReviews RCV001533161 SCV001748980 not provided Familial hemiplegic migraine no assertion provided literature only Lowest frequency (64%) of attacks of hemiplegic migraine

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