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