ClinVar Miner

Submissions for variant NM_001165963.4(SCN1A):c.2177-8dup

dbSNP: rs747086735
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000389705 SCV000417801 likely benign Epilepsy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000295837 SCV000417802 likely benign Familial hemiplegic migraine 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000958879 SCV001105763 likely benign not provided 2017-07-11 criteria provided, single submitter clinical testing

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