ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.264C>T (p.Asp88=)

gnomAD frequency: 0.00003  dbSNP: rs367543127
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001424254 SCV001626848 likely benign Landau-Kleffner syndrome 2022-08-09 criteria provided, single submitter clinical testing
Psychiatry Genetics Yale University RCV000084747 SCV000116883 not provided not provided no assertion provided not provided

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