rs1553510492, TBR1

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Seizures
CUI: C0036572
Disease: Seizures
0.700 CausalMutation CLINVAR
Moderate global developmental delay
CUI: C2237142
Disease: Moderate global developmental delay
0.700 CausalMutation CLINVAR
Aplasia/Hypoplasia of the corpus callosum
0.700 CausalMutation CLINVAR
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
0.700 CausalMutation CLINVAR
Moderate global developmental delay
CUI: C2237142
Disease: Moderate global developmental delay
0.700 GeneticVariation CLINVAR