rs671, ALDH2

N. diseases: 116
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.040 GeneticVariation BEFREE In addition to the genotypes of rs671, the patients were assessed with the PD sleep scale-2nd version (PDSS-2) and the Epworth sleepiness scale (ESS) for symptoms of daytime and nocturnal sleep disturbances. 31831791 2019
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.040 GeneticVariation BEFREE In the recessive model, the AA genotype of ALDH2 Glu487Lys showed a 4.87-fold increase (95%CI = 1.54-18.03) in the risk of Parkinson's disease when compared to the GG and GA genotypes. 27706693 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.040 GeneticVariation BEFREE This study aims to explore whether Parkinson's disease (PD) patients with reduced ALDH2 activity owing to the rs671 polymorphism are at risk for neuropsychological impairments. 27453488 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.040 GeneticVariation BEFREE Further analysis presented a significant association between haplotype frequencies and the risk for PD, primarily driven by the preponderance of the C-T-A (p = 0.03) or C-T-G (p = 0.003) haplotype of rs4767944, rs441, and rs671 in PD patients. 26130061 2015