ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.864G>A (p.Val288=)

gnomAD frequency: 0.00001  dbSNP: rs770852927
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001704285 SCV000527351 likely benign not provided 2020-04-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002059610 SCV002410104 benign Intellectual disability, autosomal dominant 8 2023-12-18 criteria provided, single submitter clinical testing

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