ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.426T>G (p.Ser142=)

gnomAD frequency: 0.00001  dbSNP: rs367543125
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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 RCV001464335 SCV001668301 likely benign Landau-Kleffner syndrome 2023-09-22 criteria provided, single submitter clinical testing
Psychiatry Genetics Yale University RCV000084745 SCV000116881 not provided not provided no assertion provided not provided

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