ClinVar Miner

Submissions for variant NM_021956.5(GRIK2):c.1285T>A (p.Ser429Thr)

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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 RCV003135460 SCV003815173 uncertain significance not provided 2020-08-11 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004753662 SCV005348393 likely benign GRIK2-related disorder 2024-09-05 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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