ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3896C>G (p.Pro1299Arg)

dbSNP: rs1156972587
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001330047 SCV001521638 uncertain significance Landau-Kleffner syndrome 2020-05-05 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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