ClinVar Miner

Submissions for variant NM_020988.3(GNAO1):c.27G>A (p.Glu9=) (rs139334934)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000585431 SCV000633981 likely benign not provided 2019-02-04 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000585431 SCV000692856 uncertain significance not provided 2017-08-01 criteria provided, single submitter clinical testing
Ambry Genetics RCV000718619 SCV000849483 likely benign History of neurodevelopmental disorder 2016-07-25 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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