ClinVar Miner

Submissions for variant NM_001165963.4(SCN1A):c.*878dup

dbSNP: rs886055037
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
Illumina Laboratory Services, Illumina RCV000285778 SCV000417745 uncertain significance Epilepsy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000343030 SCV000417746 uncertain significance Familial hemiplegic migraine 2016-06-14 criteria provided, single submitter clinical testing

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