ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.1632+17_1632+23del

dbSNP: rs756425137
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522305 SCV001731821 benign Intellectual disability, autosomal dominant 8 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001647318 SCV001861025 benign not provided 2016-03-01 criteria provided, single submitter clinical testing

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