ClinGen Knowledge Base | Clinical Genome Resource

GRIN2B

Name: GRIN2B
HGNC ID: HGNC:4586
Cytogenetic Location: 12p13.1
Haploinsufficiency: Sufficient Evidence
Triplosensitivity: No Evidence

External Resources: View external resources
ClinVar Variants: View ClinVar Variants
GeneReviews®: View GeneReviews

GRIN2B - intellectual disability, autosomal dominant 6 | MONDO:0013509

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Sufficient Evidence for Haploinsufficiency	09/11/2017	View report

GRIN2B

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Sufficient Evidence for Haploinsufficiency	09/11/2017	View report
Gene Dosage Sensitivity	No Evidence for Triplosensitivity	09/11/2017	View report

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