rs4680, COMT;MIR4761

N. diseases: 249
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Marijuana Abuse
CUI: C0024809
Disease: Marijuana Abuse
0.100 GeneticVariation BEFREE <i>COMT</i> rs4680 (Val158Met) genotype moderates the effect of cannabis on the age of onset of psychosis (AoP). 29201551 2017
Premature Ejaculation
CUI: C0033038
Disease: Premature Ejaculation
0.010 GeneticVariation BEFREE 1 COMT gene-linked locus that was associated with PE symptoms in the present study, rs4680, is a well-documented functional polymorphism that causes a valine-to-methionine substitution. 29198511 2017
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE 64 BD type I patients (39 in manic and 25 in depressive episodes) and 75 healthy controls were genotyped for COMT rs4680 and assessed for FER using the Ekman 60 Faces (EK60) and Emotion Hexagon (Hx) tests. 22222175 2012
Antisocial Personality Disorder
CUI: C0003431
Disease: Antisocial Personality Disorder
0.010 GeneticVariation BEFREE Psychopathy trait scores were assessed [total scores and 'emotional dysfunction' (also referred to as 'affective') scores] and the MAOA 30-bp variable number of tandem repeats, SLC6A4 44-bp insertion/deletion and COMT Val158Met variants were genotyped. 19829167 2009
Anorexia Nervosa
CUI: C0003125
Disease: Anorexia Nervosa
0.060 GeneticVariation BEFREE Anorexia nervosa and the Val158Met polymorphism of the COMT gene: meta-analysis and new data. 22366815 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
0.100 GeneticVariation BEFREE Val158Met Polymorphism in catechol-O-methyltransferase gene associated with risk factors for breast cancer. 14504192 2003
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
0.100 GeneticVariation BEFREE Val158Met Polymorphism in catechol-O-methyltransferase gene associated with risk factors for breast cancer. 14504192 2003
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
0.040 GeneticVariation BEFREE Val158Met is a common single-nucleotide polymorphism of the COMT gene (Ex4-12 G>A; rs4680) that results in a lower activity enzyme, increasing susceptibility to tumorigenesis. 17636223 2007
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.100 GeneticVariation BEFREE Val158Met has been found to predict performance on dopamine-mediated prefrontal tasks in healthy adults and patients with schizophrenia. 17924258 2008
Panic Disorder
CUI: C0030319
Disease: Panic Disorder
0.100 GeneticVariation BEFREE rs4680 in COMT and rs3219151 in GABRA6 showed positive associations with PD and MDD. 25974322 2015
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
0.100 GeneticVariation BEFREE rs4680 in COMT and rs3219151 in GABRA6 showed positive associations with PD and MDD. 25974322 2015
Hypersomnia
CUI: C0917799
Disease: Hypersomnia
0.010 GeneticVariation BEFREE Val158Met polymorphism in the COMT gene is associated with hypersomnia and mental health-related quality of life in a Colombian sample. 28235603 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
0.100 GeneticVariation BEFREE A valine-108-methionine polymorphism in exon 4 of the catechol-O-methyltransferase (COMT) gene causes a 3- to 4-fold reduction in enzyme activity and has been associated with an increased risk of breast cancer. 11142424 2000
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
0.100 GeneticVariation BEFREE A valine-108-methionine polymorphism in exon 4 of the catechol-O-methyltransferase (COMT) gene causes a 3- to 4-fold reduction in enzyme activity and has been associated with an increased risk of breast cancer. 11142424 2000
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
0.100 GeneticVariation BEFREE A case-control study was conducted to assess the associations between soy isoflavone intake and the CYP1A1 Ile462Val, CYP1B1 Val432Leu, and COMT Val158Met polymorphisms and breast cancer, as well as their combined effects on breast cancer. 21438753 2011
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
0.100 GeneticVariation BEFREE A case-control study was conducted to assess the associations between soy isoflavone intake and the CYP1A1 Ile462Val, CYP1B1 Val432Leu, and COMT Val158Met polymorphisms and breast cancer, as well as their combined effects on breast cancer. 21438753 2011
Anxiety
CUI: C0003467
Disease: Anxiety
0.100 GeneticVariation BEFREE A coding variant in one such gene, encoding the dopamine catabolic enzyme catechol-O-methyltransferase (COMT Val158Met), has previously been associated with anxiety and with anxiety-related temperament and altered neural responses to affective stimuli in healthy individuals. 18729643 2008
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
0.100 GeneticVariation BEFREE A coding variant in one such gene, encoding the dopamine catabolic enzyme catechol-O-methyltransferase (COMT Val158Met), has previously been associated with anxiety and with anxiety-related temperament and altered neural responses to affective stimuli in healthy individuals. 18729643 2008
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.100 GeneticVariation BEFREE A common amino-acid polymorphism in COMT, valine-108-methionine, results in a low activity form of the enzyme which we hypothesised may influence susceptibility to IPD. 8941353 1996
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.100 GeneticVariation BEFREE A common functional polymorphism (rs4680, Val158Met) has been extensively tested for an association with schizophrenia, but with conflicting results. 17482701 2007
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.100 GeneticVariation BEFREE A common Val->Met polymorphism (rs4680) in the COMT gene, associated with increased prefrontal dopamine catabolism, impairs prefrontal cognition and might increase risk for schizophrenia. 21999147 2011
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.100 GeneticVariation BEFREE A different genomic region composed of three SNPs (rs737865, rs4680, rs165599) within the COMT gene has been reported to be significantly associated with schizophrenia in Ashkenazi Jews. 19369177 2009
Impulsive Behavior
CUI: C0021125
Disease: Impulsive Behavior
0.080 GeneticVariation BEFREE A form of impulsivity, the tendency to choose immediate over delayed rewards (delay-discounting) has been associated with a single nucleotide polymorphism (SNP) in the catechol-O-methyltransferase (COMT) gene (COMTval¹⁵⁸met; rs4680). 22349272 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
0.100 GeneticVariation BEFREE A functional Val158Met polymorphism in the COMT gene has been known as a susceptible marker for breast cancer. 17047485 2006
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
0.100 GeneticVariation BEFREE A functional Val158Met polymorphism in the COMT gene has been known as a susceptible marker for breast cancer. 17047485 2006