ClinVar Miner

Submissions for variant NM_020732.3(ARID1B):c.1043_1045CAG[4] (p.Ala350dup) (rs797045267)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000717897 SCV000848757 likely benign History of neurodevelopmental disorder 2017-07-21 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 RCV000443657 SCV000510938 uncertain significance not provided 2016-10-27 criteria provided, single submitter clinical testing Converted during submission to Uncertain significance.
Genetic Services Laboratory, University of Chicago RCV000193569 SCV000246497 likely benign not specified 2015-10-22 criteria provided, single submitter clinical testing

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