ClinVar Miner

Submissions for variant NM_001040142.2(SCN2A):c.5545G>C (p.Gly1849Arg)

dbSNP: rs1553463708
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000585473 SCV000693008 uncertain significance not provided 2017-10-31 criteria provided, single submitter clinical testing

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