ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.2444G>A (p.Gly815Glu)

dbSNP: rs1833698535
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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 RCV001063640 SCV001228497 uncertain significance Intellectual disability, autosomal dominant 8 2021-09-01 criteria provided, single submitter clinical testing
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare RCV001063640 SCV001468181 likely pathogenic Intellectual disability, autosomal dominant 8 2020-06-17 no assertion criteria provided clinical testing

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