ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3153T>C (p.Tyr1051=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003456918 SCV004184533 likely benign not provided 2023-11-01 criteria provided, single submitter clinical testing GRIN2A: PM2:Supporting, BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV003741355 SCV004509660 likely benign Landau-Kleffner syndrome 2023-01-26 criteria provided, single submitter clinical testing

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