ClinVar Miner

Submissions for variant NM_020732.3(ARID1B):c.342_344GCA[8] (p.Gln131dup) (rs587779743)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000715668 SCV000846498 likely benign History of neurodevelopmental disorder 2017-05-30 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Other strong data supporting benign classification
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000430336 SCV000510639 benign not provided 2017-01-12 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000430336 SCV000610044 likely benign not provided 2017-03-17 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000114270 SCV000147829 likely benign not specified 2014-05-12 criteria provided, single submitter clinical testing

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