ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3339T>C (p.Pro1113=)

dbSNP: rs2141133304
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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 RCV002189164 SCV002489719 likely benign Landau-Kleffner syndrome 2023-11-27 criteria provided, single submitter clinical testing

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