Gene: COMT ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.430 Biomarker disease BEFREE The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome. 26919535 2016
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.430 GeneticVariation disease BEFREE Significant interaction effects were observed for maternal MTHFR 677 TT, CBS rs234715 GT + TT, and child COMT 472 AA genotypes, with greater risk for autism when mothers did not report taking prenatal vitamins periconceptionally (4.5 [1.4-14.6]; 2.6 [1.2-5.4]; and 7.2 [2.3-22.4], respectively). 21610500 2011
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.430 Biomarker disease CTD_human Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism. 16917939 2006
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.430 GeneticVariation disease BEFREE No association was observed between the COMT and DRD4 polymorphisms and autism in this sample. 11378854 2001
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.430 Biomarker disease HPO