OPRM1, opioid receptor mu 1, 4988

N. diseases: 370; N. variants: 42
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6902403
rs6902403
Entrez Id: 4988;26034
Gene Symbol: OPRM1;IPCEF1
OPRM1;IPCEF1
CUI: C0242510
Disease:
Drug usage
0.010 GeneticVariation BEFREE <b>Conclusion:</b> Dosage of methadone, plasma methadone concentration, several SNPs (rs3192723, rs6912029, rs6902403) of the <i>OPRM1</i> gene, and age of first drug use were associated with better MMT outcomes. 30420869 2018
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0524662
Disease:
Opiate Addiction
0.100 GeneticVariation BEFREE <i>OPRM1</i> nonsynonymous single nucleotide polymorphism rs1799971 (A118G) is the most prominent candidate due to its significant association with onset and treatment of opioid addiction. 31819591 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0030193
Disease:
Pain
0.100 GeneticVariation BEFREE A118G single nucleotide polymorphism of human mu-opioid receptor gene influences pain perception and patient-controlled intravenous morphine consumption after intrathecal morphine for postcesarean analgesia. 18719451 2008
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0030193
Disease:
Pain
0.100 GeneticVariation BEFREE A118G: We found that the variant G allele was associated with reduced antinociceptive effect as measured by pain tolerance thresholds to single electrical nerve stimulation (8% increase vs. 25% for the wild-type carriers, P = 0.007). 19845769 2010
dbSNP: rs1799972
rs1799972
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0242510
Disease:
Drug usage
0.010 GeneticVariation BEFREE A C17T polymorphism in the mu opiate receptor is associated with quantitative measures of drug use in African American women. 21070507 2012
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0030193
Disease:
Pain
0.100 GeneticVariation BEFREE A common single nucleotide polymorphism (SNP), A118G, in the mu-opioid receptor gene can affect opioid function and, consequently, has been suggested to contribute to individual variability in pain management and drug addiction. 20074870 2010
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1510472
Disease:
Drug Dependence
0.060 GeneticVariation BEFREE A common single nucleotide polymorphism (SNP), A118G, in the mu-opioid receptor gene can affect opioid function and, consequently, has been suggested to contribute to individual variability in pain management and drug addiction. 20074870 2010
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0001956
Disease:
Alcohol Use Disorder
0.070 GeneticVariation BEFREE A functional polymorphism of the mu-opioid receptor gene (OPRM1 A118G, rs1799971) may alter the risk of developing AUD. 29497164 2018
dbSNP: rs2236256
rs2236256
Entrez Id: 4988;26034
Gene Symbol: OPRM1;IPCEF1
OPRM1;IPCEF1
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia
C 0.800 GeneticVariation GWASCAT A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274 2014
dbSNP: rs2236256
rs2236256
Entrez Id: 4988;26034
Gene Symbol: OPRM1;IPCEF1
OPRM1;IPCEF1
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia
C 0.800 GeneticVariation GWASDB A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274 2014
dbSNP: rs2236256
rs2236256
Entrez Id: 4988;26034
Gene Symbol: OPRM1;IPCEF1
OPRM1;IPCEF1
CUI: C0855095
Disease:
Small Lymphocytic Lymphoma
C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274 2014
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0852733
Disease:
Completed Suicide
0.020 GeneticVariation BEFREE A recent genetic association study in a sample of suicide victims reported a protective effect of the G allele of Asn40Asp (rs1799971) on risk for completed suicide. 22211341 2012
dbSNP: rs3778150
rs3778150
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0019337
Disease:
Heroin Dependence
0.020 GeneticVariation BEFREE A recent study suggested that a second nearby variant within OPRM1, rs3778150, is robustly associated with heroin dependence and fully explained a smaller observed association with rs1799971. 28273335 2017
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0019337
Disease:
Heroin Dependence
0.070 GeneticVariation BEFREE A recent study suggested that a second nearby variant within OPRM1, rs3778150, is robustly associated with heroin dependence and fully explained a smaller observed association with rs1799971. 28273335 2017
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1510472
Disease:
Drug Dependence
0.060 GeneticVariation BEFREE A significant association was observed between A118G polymorphism in μ opioid receptor gene and drug addiction. 22744787 2012
dbSNP: rs1799972
rs1799972
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0524662
Disease:
Opiate Addiction
0.010 GeneticVariation BEFREE A significant association was observed between the 118G allele and no association was seen with C17T polymorphism and opioid dependence. 18181266 2007
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE A significant interaction between the A118G polymorphism and age, smoking status, and family history of cancer was also found (OR = 2.25, 95 % CI 1.36-4.12; OR = 1.75, 95 % CI 1.23-2.32; OR = 3.14, 95 % CI 1.31-7.28, respectively). 22752309 2013
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE A significant interaction between the A118G polymorphism and age, smoking status, and family history of cancer was also found (OR = 2.25, 95 % CI 1.36-4.12; OR = 1.75, 95 % CI 1.23-2.32; OR = 3.14, 95 % CI 1.31-7.28, respectively). 22752309 2013
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1510472
Disease:
Drug Dependence
0.060 GeneticVariation BEFREE A single nucleotide polymorphism (SNP) in the human mu-opioid receptor gene (OPRM1 A118G) has been widely studied for its association in a variety of drug addiction and pain sensitivity phenotypes; however, the extent of these adaptations and the mechanisms underlying these associations remain elusive. 19528658 2009
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0030193
Disease:
Pain
0.100 GeneticVariation BEFREE A single nucleotide polymorphism (SNP) in the human mu-opioid receptor gene (OPRM1 A118G) has been widely studied for its association in a variety of drug addiction and pain sensitivity phenotypes; however, the extent of these adaptations and the mechanisms underlying these associations remain elusive. 19528658 2009
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic
0.100 GeneticVariation BEFREE A single-nucleotide polymorphism (SNP) within the OPRM1 gene, A118G, leading to an amino acid change (Asn40Asp) in the extracellular portion of the receptor, has been implicated in alcoholism as well as in drug addiction, pain sensitivity and stress response, and in animal and human studies relates to the alcohol-dependent phenotype as well as to the treatment response to the µ-opioid antagonist naltrexone. 23543091 2014
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1510472
Disease:
Drug Dependence
0.060 GeneticVariation BEFREE A single-nucleotide polymorphism (SNP) within the OPRM1 gene, A118G, leading to an amino acid change (Asn40Asp) in the extracellular portion of the receptor, has been implicated in alcoholism as well as in drug addiction, pain sensitivity and stress response, and in animal and human studies relates to the alcohol-dependent phenotype as well as to the treatment response to the µ-opioid antagonist naltrexone. 23543091 2014
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0033975
Disease:
Psychotic Disorders
0.010 GeneticVariation BEFREE A subdivision of our MAP group revealed that A118G of OPRM shows a significant association with MAP psychosis having latency less than three years. 15542732 2004
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0349204
Disease:
Nonorganic psychosis
0.010 GeneticVariation BEFREE A subdivision of our MAP group revealed that A118G of OPRM shows a significant association with MAP psychosis having latency less than three years. 15542732 2004
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0028043
Disease:
Nicotine Dependence
0.030 GeneticVariation BEFREE A systematic review of the A118G (Asn40Asp) variant of OPRM1 in relation to smoking initiation, nicotine dependence and smoking cessation. 22676196 2012