ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.306C>T (p.Asp102=)

gnomAD frequency: 0.00006  dbSNP: rs200850130
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000710140 SCV000527650 likely benign not provided 2021-02-01 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000710140 SCV000613548 benign not provided 2017-10-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000550789 SCV000638240 likely benign Landau-Kleffner syndrome 2024-01-05 criteria provided, single submitter clinical testing

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