Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4680
rs4680
0.090 GeneticVariation BEFREE Previous research shows that OCD is associated with serotonin-related polymorphisms (5-HTTLPR coded as triallelic and HTR2A rs6311/rs6313) and, in males, a polymorphism involved in catecholamine modulation; COMT (rs4680). 26616111

2016

dbSNP: rs4680
rs4680
0.090 GeneticVariation BEFREE A sample of 199 patients with OCD and 200 healthy individuals was genotyped for -287A > G (rs2075507) and Val158Met (rs4680) single nucleotide polymorphisms (SNPs) by TaqMan(®) or restriction mapping. 26687156

2016

dbSNP: rs4680
rs4680
0.090 GeneticVariation BEFREE The present case-control/pharmacogenetic study did not provide clear evidence that the COMT Val158Met polymorphism is a predictor of OCD or of OCD patients' clinical responses. 26010653

2015

dbSNP: rs4680
rs4680
0.090 GeneticVariation BEFREE Therefore, the purpose of our study was to assess COMT activity in OCD by measuring plasma levels of 3-O-methyl-dopa (3-OMD), which result from the methylation of levodopa by COMT, and to investigate the relationship between 3-OMD levels and the V158M polymorphism. 19676096

2010

dbSNP: rs4680
rs4680
0.090 GeneticVariation BEFREE There was a trend for an association of the COMT 158Met allele with OCD i</span>n males, and an interaction between the COMT Val158Met genotype and sex on the somatic and sensory phenomena symptom dimension, with females showing lower scores. 19521967

2010

dbSNP: rs4680
rs4680
0.090 GeneticVariation BEFREE A haplotype composed of three SNPs [rs2097603; rs4680 (158Val/Met); rs165599] representing the major linkage disequilibrium blocks in COMT and previously implicated in functional variation, was found to be associated with ADHD and OCD in 22q11.2DS individuals. 17949513

2008

dbSNP: rs4680
rs4680
0.090 GeneticVariation BEFREE In subjects of Afrikaner descent, the L/L genotype of the COMT Val158Met polymorphism was significantly more common in the OCD hoarding group, with a preponderance of low activity alleles, compared with nonhoarding patients and controls. 16187774

2005

dbSNP: rs4680
rs4680
0.090 GeneticVariation BEFREE These results do not support the hypothesis that the COMT Val158Met gene polymorphism is associated with liability to schizophrenia-OCD. 16043283

2005

dbSNP: rs4680
rs4680
0.090 GeneticVariation BEFREE This polymorphism (valine to methionine at codon 158) has been previously reported to influence the activity of COMT by three to four-fold and has recently been reported to be associated with OCD.1 We tested for linkage using an autosomal dominant model with reduced penetrance and non-parametric methods. 10523824

1999