ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1308T>C (p.Cys436=)

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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 RCV003077490 SCV003463321 likely benign Landau-Kleffner syndrome 2023-12-11 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV004598237 SCV005092754 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing GRIN2A: PM2:Supporting, BP4, BP7

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