ClinVar Miner

Submissions for variant NM_001165963.4(SCN1A):c.*672_*675del

dbSNP: rs886055038
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000365260 SCV000417749 uncertain significance Familial hemiplegic migraine 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000392480 SCV000417750 uncertain significance Epilepsy 2016-06-14 criteria provided, single submitter clinical testing

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