ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.22A>C (p.Thr8Pro)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille RCV000681504 SCV000808954 likely benign Intellectual disability 2017-01-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001060033 SCV001224694 benign Intellectual disability, autosomal dominant 8 2022-02-04 criteria provided, single submitter clinical testing

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