ClinVar Miner

Submissions for variant NM_015176.4(FBXO28):c.13_14delinsAA (p.Ala5Lys)

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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 Hospital of Duesseldorf RCV003336634 SCV004046701 uncertain significance Developmental and epileptic encephalopathy 100 criteria provided, single submitter not provided

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