ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.4261G>T (p.Asp1421Tyr)

dbSNP: rs1567275051
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV000767350 SCV000897920 uncertain significance Landau-Kleffner syndrome 2018-12-18 criteria provided, single submitter clinical testing

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