ClinVar Miner

Submissions for variant NM_020732.3(ARID1B):c.1032_1034GGC[5] (p.Ala350dup) (rs764418312)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000719872 SCV000850743 likely benign History of neurodevelopmental disorder 2016-06-29 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Other strong data supporting benign classification
Gharavi Laboratory,Columbia University RCV000722971 SCV000854102 uncertain significance not provided 2018-09-16 no assertion criteria provided research

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