ClinVar Miner

Submissions for variant NM_001320.7(CSNK2B):c.467G>A (p.Gly156Asp)

dbSNP: rs2151188873
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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 Medical Genetics, National & Kapodistrian University of Athens RCV001842238 SCV002102413 pathogenic Poirier-Bienvenu neurodevelopmental syndrome 2022-03-03 criteria provided, single submitter clinical testing
Baylor Genetics RCV001842238 SCV003835107 uncertain significance Poirier-Bienvenu neurodevelopmental syndrome 2021-12-21 criteria provided, single submitter clinical testing

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