ClinVar Miner

Submissions for variant NM_001320.7(CSNK2B):c.73-1G>A

dbSNP: rs2151185341
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Stanford Center for Inherited Cardiovascular Disease, Stanford University RCV002255105 SCV002037157 likely pathogenic Poirier-Bienvenu neurodevelopmental syndrome 2021-07-01 criteria provided, single submitter clinical testing

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