ClinVar Miner

Submissions for variant NM_020732.3(ARID1B):c.5802C>T (p.Ile1934=) (rs142499766)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000192586 SCV000246536 benign not specified 2018-05-01 criteria provided, single submitter clinical testing
Ambry Genetics RCV000719915 SCV000850787 likely benign History of neurodevelopmental disorder 2016-03-23 criteria provided, single submitter clinical testing
Invitae RCV000871463 SCV001013128 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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