ClinVar Miner

Submissions for variant NM_177559.3(CSNK2A1):c.213+45T>C

gnomAD frequency: 0.00364  dbSNP: rs181461026
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001553023 SCV001773818 likely benign not provided 2018-12-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001553023 SCV004700599 benign not provided 2024-04-01 criteria provided, single submitter clinical testing CSNK2A1: BP4, BP7, BS1, BS2

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