ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.2007+20C>G

dbSNP: rs1013909512
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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 RCV002208412 SCV002493918 likely benign Landau-Kleffner syndrome 2021-07-14 criteria provided, single submitter clinical testing

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