rs1229984, ADH1B

N. diseases: 83
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Alcohol Use Disorder
CUI: C0001956
Disease: Alcohol Use Disorder
0.060 GeneticVariation BEFREE With longitudinal EHR data from the Million Veteran Program (MVP) linked to genetic data, we used two population-specific polymorphisms in ADH1B that are associated strongly with AUD in African Americans (AAs) and European Americans (EAs): rs2066702 (Arg369Cys, AAs) and rs1229984 (Arg48His, EAs) as criterion measures. 29972609 2018
Alcohol Use Disorder
CUI: C0001956
Disease: Alcohol Use Disorder
0.060 GeneticVariation BEFREE Therefore, among those at risk for greater consumption, e.g. those who experienced childhood adversity, ADH1B-rs1229984 appears to have a stronger effect on alcohol consumption and consequently on risk for AUD symptom severity. 24164917 2015
Alcohol Use Disorder
CUI: C0001956
Disease: Alcohol Use Disorder
0.060 GeneticVariation BEFREE A significant rs1229984 by childhood adversity interaction was observed for AUD symptoms in EA men. 25410943 2014
Alcohol Use Disorder
CUI: C0001956
Disease: Alcohol Use Disorder
0.060 GeneticVariation BEFREE This is the first study to show that ADH1B rs1229984 is related to 6 of the 11 DSM-IV AUD criteria and that alcohol consumption explained a significant proportion of these associations and the association of ADH1B with AUDs. 24988262 2014
Alcohol Use Disorder
CUI: C0001956
Disease: Alcohol Use Disorder
0.060 GeneticVariation BEFREE The functional variant rs1229984 in alcohol dehydrogenase 1B (ADH1B) has been associated at a genome-wide level with alcohol use disorders in diverse adult populations. 25257461 2014
Alcohol Use Disorder
CUI: C0001956
Disease: Alcohol Use Disorder
0.060 GeneticVariation BEFREE Lack of the ADH1B rs1229984 protective allele was significantly associated with consumption- and AUD-related phenotypes (OR = 1.77 for AUD; OR = 1.83 for risk drinking), while lack of the ADH1C rs698 protective allele was significantly associated with AUD-related phenotypes (OR = 2.32 for AUD). 23895337 2013