ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1802T>C (p.Ile601Thr)

dbSNP: rs1404462639
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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 RCV001366489 SCV001562791 benign Landau-Kleffner syndrome 2022-08-15 criteria provided, single submitter clinical testing

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