ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.4022G>T (p.Ser1341Ile)

dbSNP: rs757898035
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001438419 SCV001641291 likely benign Landau-Kleffner syndrome 2020-10-09 criteria provided, single submitter clinical testing

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