ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3447C>T (p.Asp1149=)

dbSNP: rs2141132170
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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 RCV001452855 SCV001656530 likely benign Landau-Kleffner syndrome 2022-08-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001726558 SCV001961571 likely benign not provided 2021-08-01 criteria provided, single submitter clinical testing

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