rs9551963, ALOX5AP

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
0.020 GeneticVariation BEFREE We found no association of the <i>ALOX5AP</i> rs10507391 (OR=1.03 for A allele vs T allele; 95% CI: 0.93-1.14; <i>P</i>=0.557), rs4769874 (OR=1.13 for A allele vs G allele; 95% CI: 1.00-1.28; <i>P</i>=0.050), rs9551963 (OR=1.03 for A allele vs C allele; 95% CI: 0.96-1.11; <i>P</i>=0.372), rs17222814 (OR=1.09 for A allele vs G allele; 95% CI: 0.96-1.24; <i>P</i>=0.195), rs17222919 (OR=0.89 for G allele vs T allele; 95% CI: 0.75-1.06; <i>P</i>=0.175), and rs4073259 (OR=1.20 for A allele vs G allele; 95% CI: 1.00-1.45; <i>P</i>=0.056) polymorphisms with IS risk. 30774347 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
0.020 GeneticVariation BEFREE These results suggest the ALOX5AP SNP A allele in rs4073259 and genotype rs9579646 GG, rs9551963 AC, and haplotype rs9315050 & rs9551963 AAAC were associated with an increased risk of ischemic stroke in the Han population, while rs4073259 GG was associated with a decreased risk. 22849376 2012