ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.144G>A (p.Glu48=)

dbSNP: rs1334555320
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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 RCV001421887 SCV001624419 likely benign Landau-Kleffner syndrome 2020-08-25 criteria provided, single submitter clinical testing

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