ClinVar Miner

Submissions for variant NM_152221.3(CSNK1E):c.885+1G>A

dbSNP: rs1569077009
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Wu Jinyu Laboratory, Institute of Genomic Medicine, Wenzhou Medical University RCV000721134 SCV000844977 pathogenic Developmental and epileptic encephalopathy, 1 no assertion criteria provided clinical testing

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