Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3810950
rs3810950
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.070 GeneticVariation BEFREE Our findings are consistent with the results of the meta-analytical studies of the relationship between rs3810950 polymorphism and AD and provide further material evidence for a direct (primary) involvement of cholinergic mechanisms in the etiopathogenesis of AD, particularly as a factor in cognitive decline and perturbed conscious awareness commonly observed in patients with AD. 29759072

2018

dbSNP: rs3810950
rs3810950
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.070 GeneticVariation BEFREE The rs3810950G/A polymorphism had a negative effect on the risk of AD for GA or GG+GA genotypes compared with AA in the overall population or Asians. 27390868

2016

dbSNP: rs3810950
rs3810950
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.070 GeneticVariation BEFREE Pooled results of our meta-analysis indicated CHAT rs2177369 polymorphism was correlated with decreasing AD risk in one of five genetic models (dominant: OR = 0.77, 95% CI: 0.62-0.96), while rs3810950 mutant was associated with AD development in three models (allelic: OR = 1.18, 95% CI: 1.01-1.37, homozygous: OR = 1.63, 95% CI: 1.09-2.42, and recessive: OR = 1.65, 95% CI: 1.20-2.26). 27597977

2016

dbSNP: rs3810950
rs3810950
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.070 GeneticVariation BEFREE For CHAT, rs2177369 (G>A) in whites and rs3810950 (G>A) in Asians were found to be associated with AD susceptibility. 27272392

2016

dbSNP: rs3810950
rs3810950
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.070 GeneticVariation BEFREE Stratification by the presence of the APOE ε4 allele showed that rs3810950 AG/non-APOE ε4 carriers and rs3810950 AA/APOE ε4 carriers were associated with a lower cognitive composite score in younger elderly 73-83 years of age, similar to previous reports of association with AD. 21883924

2011

dbSNP: rs3810950
rs3810950
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.070 GeneticVariation BEFREE Nominal allelic and genotypic associations with AD r</span>isk in the cross-sectional VITA sample were found for rs3810950 (p = 0.038 for genotype, OR = 1.66 95% CI 1.03-2.68, p = 0.052 allele-wise). 21507424

2011

dbSNP: rs3810950
rs3810950
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.070 GeneticVariation BEFREE Previous studies have reported significant disease associations for both the K-variant of BChE and the coding ChAT rs3810950 polymorphism with AD. 15690550

2005