ClinVar Miner

Submissions for variant NM_000834.4(GRIN2B):c.2664C>T (p.Thr888=) (rs1806201)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000715260 SCV000846088 benign History of neurodevelopmental disorder 2016-01-08 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000084728 SCV000842282 benign not provided 2017-04-20 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000117194 SCV000151358 likely benign not specified no assertion criteria provided clinical testing Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed.
Illumina Clinical Services Laboratory,Illumina RCV000377659 SCV000377113 likely benign Intellectual Disability, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Psychiatry Genetics Yale University RCV000084728 SCV000116864 not provided not provided no assertion provided not provided

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