Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6269
rs6269
0.010 GeneticVariation BEFREE The rs6269 was borderline for myofascial pain (OR<sub>c</sub>  = 1.82; CI 95%: 0.92-3.59; P = 0.08) and disc displacement (OR<sub>c</sub>  = 2.38; CI 95% 0.95-5.97; P = 0.06) and also was associated with anxiety (OR<sub>a</sub>  = 2.34; CI 95% 1.04-5.25; P = 0.03). 30811655

2019

dbSNP: rs165599
rs165599
0.010 GeneticVariation BEFREE Individual COMT SNPs (val158met, rs737865, and rs165599) modulated the association between antenatal maternal anxiety and the prefrontal and parietal cortical thickness in neonates. 25320962

2015

dbSNP: rs61910731
rs61910731
0.010 GeneticVariation BEFREE We show that Val/Val but neither Met/Met nor Val/Met carriers of the catechol-O-methyltransferase (COMT) Val(158)Met polymorphism-a prime candidate for anxiety vulnerability-became significantly more anxious during the fMRI experiment (N=97 females: 24 Val/Val, 51 Val/Met, and 22 Met/Met). 25238960

2014

dbSNP: rs75012854
rs75012854
0.010 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875

2004

dbSNP: rs774847933
rs774847933
0.010 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875

2004

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Heterosis in COMT Val158Met Polymorphism Contributes to Sex-Differences in Children's Math Anxiety. 31156495

2019

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Similar findings were observed in the PREDO cohort where maternal prenatal anxiety interacted with child rs4680 to predict symptoms of ADHD at 3.5 years of age. 28614354

2017

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Analyses suggest that COMT val158met moderates the influence of early life stress on preschool-age symptoms of anxiety. 28859863

2017

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Thus, our results provide further evidence that 5-HTTLPR and COMT Val(158)Met genotypes influence the vulnerability for the development of anxiety disorders via different mechanisms. 25455425

2015

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Applying a multilevel approach, we analyzed the main and interactive effects of the functional COMT val158met polymorphism and L-dopa (single-dose 50 mg levodopa and 12.5 mg carbidopa; double-blind, placebo-controlled design) on the emotion-potentiated (unpleasant, neutral, and pleasant IAPS pictures) startle response as an intermediate phenotype of anxiety in a sample of 100 healthy probands (f = 52, m = 48). 25510857

2015

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Based on haplotype trend regression analysis, findings also showed that among rs737865-val158met-rs165599 haplotypes, the A-val-G (AGG) haplotype probabilities modulated positive associations of antenatal maternal anxiety with cortical thickness in the right ventrolateral prefrontal cortex and the right superior parietal cortex and precuneus. 25320962

2015

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE We also found a significant interaction effect of COMT met alleles (β = -32.5 SE 14.1, P = 0.021). in patients genotyped for COMT val158met (N  = 87) specifically COMT × conscientiousness (β = 0.73 SE 0.26, P = 0.0042) and COMT × anxiety (β = -0.42 SE 0.16, P = 0.0078) interaction effects. 25722948

2015

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE We investigated and provided evidence of lower PPI: (i) in healthy pregnant women compared to healthy non-pregnant controls, (ii) in pregnant women with anxiety disorders compared to healthy pregnant women, (iii) in pregnant women with anxiety disorders using SSRI compared to un-medicated pregnant women with anxiety disorders, and (iv) in healthy pregnant women carrying the COMT Val158Met Val/Val genotype compared to Met carriers. 26189199

2015

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE This meta-analysis provides evidence for sex and ethnic differences in the association of the COMT val158met polymorphism with anxiety traits. 24300663

2014

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE We show that Val/Val but neither Met/Met nor Val/Met carriers of the catechol-O-methyltransferase (COMT) Val(158)Met polymorphism-a prime candidate for anxiety vulnerability-became significantly more anxious during the fMRI experiment (N=97 females: 24 Val/Val, 51 Val/Met, and 22 Met/Met). 25238960

2014

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE The interaction of early life experiences with COMT val158met affects anxiety sensitivity. 24118915

2013

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE COMT Val158Met was not associated with anxiety or mood disorders in either gender. 23928267

2013

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE We extended this research by investigating whether the val158met polymorphism was associated with childhood symptoms of depression and anxiety in two independent samples of young children (Ns = 476 and 409). 23475824

2013

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE We therefore examined the association of the COMT Val158Met and BDNF Val66Met polymorphisms with BP-II with and without comorbidity of AD, and possible interactions between these genes. 23026378

2013

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Results indicate a main as well as a GxE effect of the COMT Val158Met variant and childhood maltreatment on the affect-modulated startle reflex, supporting a complex pathogenetic model of the affect-modulated startle reflex as a basic neurobiological defensive reflex potentially related to anxiety and affective disorders. 22745815

2012

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE The present results provide further support for a-potentially female-specific-role of the COMT val158met polymorphism in the genetic and neural underpinnings of anxiety- and depression-related intermediate phenotypes and may aid in further clarifying the differential role of COMT genotype driven dopaminergic tonus in the processing of emotionally salient stimuli. 22387174

2012

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE The catechol-O-methyltransferase (COMT) Val158Met polymorphism has been found to affect fear extinction and might play a role in the etiology of anxiety disorders. 19944409

2010

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Association of COMT (Val158Met) and BDNF (Val66Met) gene polymorphisms with anxiety, ADHD and tics in children with autism spectrum disorder. 19582565

2009

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE In this population-based study, no clear association between the Val158Met polymorphism and depression and anxiety was revealed. 18578865

2008

dbSNP: rs4680
rs4680
0.100 GeneticVariation BEFREE Two common functional polymorphisms in catechol-O-methyltransferase (COMT Val158Met) and brain-derived neurotrophic factor (BDNF Val66Met) genes have been implicated in the neurobiology of anxiety and depression. 17941097

2008