ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.1340-18_1340-17insGTA

gnomAD frequency: 0.00721  dbSNP: rs199804460
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001572483 SCV001797133 likely benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072234 SCV002372472 benign Intellectual disability, autosomal dominant 8 2024-01-29 criteria provided, single submitter clinical testing

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