ClinVar Miner

Submissions for variant NM_000834.5(GRIN2B):c.324C>T (p.Ile108=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003131078 SCV003817472 uncertain significance not provided 2019-06-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003778706 SCV004568285 likely benign Intellectual disability, autosomal dominant 6; Developmental and epileptic encephalopathy, 27 2022-12-01 criteria provided, single submitter clinical testing

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