ClinVar Miner

Submissions for variant NM_000834.4(GRIN2B):c.465C>A (p.Ser155=) (rs115189840)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000186632 SCV000168767 benign not specified 2014-05-02 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000546271 SCV000659540 benign Mental retardation, autosomal dominant 6; Epileptic encephalopathy, early infantile, 27 2017-12-04 criteria provided, single submitter clinical testing
Psychiatry Genetics Yale University RCV000084732 SCV000116868 not provided not provided no assertion provided not provided

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