Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799971
rs1799971
0.070 GeneticVariation BEFREE Some studies show that AUD patients carrying the G-allele of the OPRM1 variant c.118A>G respond better to naltrexone, resulting in reduced relapse rates compared to carriers of the AA genotype. 30384381

2018

dbSNP: rs1799971
rs1799971
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: rs1799971
rs1799971
0.070 GeneticVariation BEFREE An association between AUD and a coding single nucleotide polymorphism (SNP) (rs1799971 encoding an Asn40Asp amino acid substitution, A118G) within the µ-opioid receptor 1 gene (OPRM1) has been reported. 25836994

2015

dbSNP: rs1799971
rs1799971
0.070 GeneticVariation BEFREE These results suggest that A118G (Asn40Asp) polymorphism may not have a major effect on the development of alcohol use disorders at least in the Finnish population. 23729673

2014

dbSNP: rs1799971
rs1799971
0.070 GeneticVariation BEFREE This study provides initial evidence that the association between the A118G SNP of the OPRM1 gene and risk of AUDs is moderated by modifiable factors. 23136901

2013

dbSNP: rs1799971
rs1799971
0.070 GeneticVariation BEFREE Male children of alcoholics were less likely to be carriers of the G allele in single nucleotide polymorphism A118G (rs1799971), and those who were homozygous for the A allele were more likely to affiliate with alcohol use promoting peers who increased the risk for AUD symptoms at all ages. 22781865

2012

dbSNP: rs1799971
rs1799971
0.070 GeneticVariation BEFREE Adolescents (n = 187; mean age = 15.4 years; 47.6% female) were genotyped for A118G (rs1799971), a single-nucleotide polymorphism (SNP) of the OPRM1 gene, and assessed for alcohol use disorder (AUD) diagnoses and other psychopathology. 19860800

2010