ClinVar Miner

Submissions for variant NM_001374828.1(ARID1B):c.1620GGCGGCGGCGGG[1] (p.541AAAG[1])

dbSNP: rs1239601972
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001572175 SCV001796771 likely benign not provided 2023-02-27 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Genetic Services Laboratory, University of Chicago RCV001815039 SCV002062017 uncertain significance not specified 2018-08-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001572175 SCV002344775 likely benign not provided 2024-11-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001572175 SCV005331149 likely benign not provided 2024-08-01 criteria provided, single submitter clinical testing ARID1B: BP3

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