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Variant Pathogenicity
FOXP1
Name
FOXP1
HGNC ID
HGNC:3823
Cytogenetic Location
3p13
Haploinsufficiency
Sufficient Evidence
Triplosensitivity
No Evidence
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ClinVar Variants
FOXP1
-
intellectual disability-severe speech delay-mild dysmorphism syndrome
| MONDO:0013352
Curated by
Classification
Date
Report
Gene-Disease Validity
Definitive
05/09/2019
View report
Gene Dosage Sensitivity
Sufficient Evidence for Haploinsufficiency
08/22/2019
View report
FOXP1
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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