ClinVar Miner

Submissions for variant NM_173354.5(SIK1):c.1582G>A (p.Gly528Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003991813 SCV004810086 likely benign Developmental and epileptic encephalopathy, 30 2024-04-04 criteria provided, single submitter clinical testing

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