ClinVar Miner

Submissions for variant NM_001320.7(CSNK2B):c.291+1G>T

dbSNP: rs2151187350
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Provincial Medical Genetics Program of British Columbia, University of British Columbia RCV002071022 SCV002320809 likely pathogenic Poirier-Bienvenu neurodevelopmental syndrome 2022-01-01 criteria provided, single submitter clinical testing

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