ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1125G>C (p.Val375=)

dbSNP: rs2141370109
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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 RCV002211857 SCV002353704 likely benign Landau-Kleffner syndrome 2023-07-07 criteria provided, single submitter clinical testing

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