ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3039G>T (p.Leu1013=)

dbSNP: rs577077724
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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 RCV002109195 SCV002438595 likely benign Landau-Kleffner syndrome 2022-11-08 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV004809785 SCV005431868 likely benign not provided 2024-09-01 criteria provided, single submitter clinical testing GRIN2A: BP4, BP7

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