ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1329-7dup

dbSNP: rs1455515948
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001496129 SCV001700820 likely benign Landau-Kleffner syndrome 2022-07-19 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001820202 SCV002068375 uncertain significance not specified 2018-02-09 criteria provided, single submitter clinical testing

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