ClinVar Miner

Submissions for variant NM_001320.7(CSNK2B):c.410G>A (p.Cys137Tyr)

dbSNP: rs2151188789
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes RCV002277666 SCV002564482 pathogenic Neurodevelopmental disorder 2022-02-21 criteria provided, single submitter clinical testing
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen RCV004596533 SCV005088612 likely pathogenic Poirier-Bienvenu neurodevelopmental syndrome 2024-07-29 criteria provided, single submitter clinical testing

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