ClinVar Miner

Submissions for variant NM_000834.5(GRIN2B):c.1103A>C (p.Asn368Thr)

dbSNP: rs1314805334
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001034520 SCV001197878 benign Intellectual disability, autosomal dominant 6; Developmental and epileptic encephalopathy, 27 2019-11-06 criteria provided, single submitter clinical testing
Centogene AG - the Rare Disease Company RCV001809956 SCV002059247 uncertain significance Intellectual disability, autosomal dominant 6 2018-11-22 criteria provided, single submitter clinical testing

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