ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.1339+7GCGCGGGGCAGGGCGCGGG[3]

dbSNP: rs761110882
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503597 SCV000595054 uncertain significance not specified 2016-11-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060118 SCV002487579 benign Intellectual disability, autosomal dominant 8 2023-10-03 criteria provided, single submitter clinical testing

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