rs165599, ARVCF;COMT

N. diseases: 27
Disease: Hallucinations ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hallucinations
CUI: C0018524
Disease: Hallucinations
0.010 GeneticVariation BEFREE The SNP rs165599, which has been mapped to the 3'-UTR region of the COMT gene, was significantly associated with schizophrenia in our family study, and possibly associated with the age of onset, delusion/hallucination symptom dimension, and CPT performance. 19369177 2009