ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.3849G>A (p.Lys1283=)

dbSNP: rs1596374942
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001467057 SCV001671074 likely benign Landau-Kleffner syndrome 2018-08-29 criteria provided, single submitter clinical testing

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