ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3432C>T (p.Asn1144=)

gnomAD frequency: 0.00002  dbSNP: rs746900457
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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 RCV003741239 SCV001128802 likely benign Landau-Kleffner syndrome 2023-04-15 criteria provided, single submitter clinical testing

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