ClinVar Miner

Submissions for variant NM_005249.5(FOXG1):c.159C>T (p.His53=) (rs769410384)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001088354 SCV000676974 likely benign Rett syndrome, congenital variant 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000658688 SCV000780474 likely benign not provided 2017-12-01 criteria provided, single submitter clinical testing
Ambry Genetics RCV000719803 SCV000850673 likely benign History of neurodevelopmental disorder 2017-05-22 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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