ClinVar Miner

Submissions for variant NM_177559.3(CSNK2A1):c.1061-9T>C

gnomAD frequency: 0.00031  dbSNP: rs371565154
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001692773 SCV001909390 benign not provided 2019-08-28 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002496010 SCV002808599 likely benign Okur-Chung neurodevelopmental syndrome 2022-04-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001692773 SCV004149738 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing CSNK2A1: PP2, BS2

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