ClinVar Miner

Submissions for variant NM_020732.3(ARID1B):c.962_964GAG[9] (p.Gly328dup) (rs747790383)

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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 RCV000718518 SCV000849382 likely benign History of neurodevelopmental disorder 2017-04-07 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 RCV000514747 SCV000610690 likely benign not provided 2017-02-27 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000193840 SCV000246546 likely benign not specified 2015-02-26 criteria provided, single submitter clinical testing

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