ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1342G>A (p.Glu448Lys)

dbSNP: rs368026708
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000730548 SCV000858294 uncertain significance not provided 2017-11-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002536449 SCV003471737 likely benign Landau-Kleffner syndrome 2025-01-25 criteria provided, single submitter clinical testing

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