ClinVar Miner

Submissions for variant NM_020732.3(ARID1B):c.1054_1056GGC[5] (p.Gly357del) (rs797045268)

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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 RCV000718674 SCV000849538 likely benign History of neurodevelopmental disorder 2017-05-09 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: In silico models in agreement (benign),Subpopulation frequency in support of benign classification
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000194869 SCV000258160 uncertain significance not specified 2015-07-21 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000194869 SCV000246498 likely benign not specified 2015-04-24 criteria provided, single submitter clinical testing

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