ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3927G>C (p.Arg1309=)

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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 RCV003089709 SCV003476032 likely benign Landau-Kleffner syndrome 2022-08-10 criteria provided, single submitter clinical testing

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