ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.42C>G (p.Ala14=)

dbSNP: rs2142391305
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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 RCV001499951 SCV001704726 likely benign Landau-Kleffner syndrome 2020-07-24 criteria provided, single submitter clinical testing

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