ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3800A>C (p.Tyr1267Ser)

dbSNP: rs1333994593
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myelin Disorders Clinic-Children's Medical Center/Medical Genetics Lab-Tarbiat Modares University, Children's Medical Center, Pediatrics Center of Excellence, RCV001260239 SCV001426655 uncertain significance Landau-Kleffner syndrome no assertion criteria provided clinical testing

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