ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1662C>T (p.Ser554=)

dbSNP: rs1596476657
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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 RCV001446951 SCV001650005 likely benign Landau-Kleffner syndrome 2022-09-03 criteria provided, single submitter clinical testing

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