ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.4103G>C (p.Cys1368Ser)

dbSNP: rs2056735436
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001253287 SCV001428933 uncertain significance Migraine, familial hemiplegic, 1 2017-09-01 criteria provided, single submitter clinical testing

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