ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.2070G>A (p.Thr690=)

gnomAD frequency: 0.00006  dbSNP: rs141924924
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001720179 SCV000523706 likely benign not provided 2021-06-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001452839 SCV001656514 likely benign Landau-Kleffner syndrome 2024-10-04 criteria provided, single submitter clinical testing

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