ClinVar Miner

Submissions for variant NM_001040142.2(SCN2A):c.2636G>T (p.Gly879Val)

dbSNP: rs1559376694
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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 RCV001253533 SCV001429289 uncertain significance Seizures, benign familial infantile, 3 2019-06-05 criteria provided, single submitter clinical testing

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