rs4680, COMT;MIR4761

N. diseases: 249
Disease: Schizophrenia, Childhood ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Schizophrenia, Childhood
CUI: C0036346
Disease: Schizophrenia, Childhood
0.010 GeneticVariation BEFREE Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls. 21620981 2011