ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.702C>T (p.Asp234=)

gnomAD frequency: 0.00001  dbSNP: rs150208429
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000457288 SCV000562533 likely benign Landau-Kleffner syndrome 2024-10-23 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000487783 SCV000575037 likely benign not provided 2021-01-01 criteria provided, single submitter clinical testing

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