ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3468A>T (p.Glu1156Asp)

dbSNP: rs778180100
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001697480 SCV000720037 likely benign not provided 2018-04-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000639604 SCV000761183 likely benign Landau-Kleffner syndrome 2024-10-28 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001821738 SCV002068176 benign not specified 2017-12-27 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001697480 SCV004141095 likely benign not provided 2022-04-01 criteria provided, single submitter clinical testing GRIN2A: BP4, BS1

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