ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.1632+14G>A

gnomAD frequency: 0.00065  dbSNP: rs200337681
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000443783 SCV000525196 likely benign not specified 2016-09-28 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV002065084 SCV002407952 benign Intellectual disability, autosomal dominant 8 2024-01-27 criteria provided, single submitter clinical testing

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