ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.2537G>A (p.Arg846His)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002592053 SCV003499577 likely benign Landau-Kleffner syndrome 2024-09-10 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003427574 SCV004141099 uncertain significance not provided 2022-08-01 criteria provided, single submitter clinical testing GRIN2A: PM2

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