ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.2762-168G>A

gnomAD frequency: 0.02820  dbSNP: rs35793467
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 RCV001592519 SCV001827120 likely benign not provided 2018-07-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001592519 SCV005226207 likely benign not provided criteria provided, single submitter not provided

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