rs165774, COMT

N. diseases: 11
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE Remarkably, alleles of <i>COMT</i> rs165774 (G), <i>DRD2</i> rs6277 (T), and <i>DRD3</i> rs6280 (C) were associated with raised predisposition to schizophrenia (all <i>P</i><0.001). 29255361 2017
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE The second-stage study showed that intronic SNP rs165774 (χ(2)  = 8.327, P = 0.0039), CNV6 (χ(2)  = 19.66, P = 0.00005), and CNV8 (χ(2)  = 16.57, P = 0.00025) were significantly associated with schizophrenia. 26852906 2016
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE Individuals with schizophrenia were more than twice as likely to carry the GG genotype compared to the AA genotype for both the rs165774 and rs4680 SNPs. 20934310 2012
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE Individuals with schizophrenia were more than twice as likely to carry the GG genotype compared to the AA genotype for both the rs165774 and rs4680 SNPs. 22208661 2011