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	08/22/2019	View report

GRIN2B

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Sufficient Evidence for Haploinsufficiency	08/22/2019	View report
Gene Dosage Sensitivity	No Evidence for Triplosensitivity	08/22/2019	View report