ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.2444-10C>T (rs200762696)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000872234 SCV001014021 likely benign not provided 2017-09-18 criteria provided, single submitter clinical testing
Invitae RCV001402303 SCV001604148 likely benign Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant 2020-11-22 criteria provided, single submitter clinical testing

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