Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1293767
rs1293767
CUI: C0004096
Disease: Asthma
Asthma
0.700 GeneticVariation GWASCAT Identification of Four Novel Loci in Asthma in European American and African American Populations. 27611488

2017

dbSNP: rs1293762
rs1293762
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.010 GeneticVariation BEFREE Data obtained suggest that the OAS2 rs1293762 and CD209 rs2287886 SNPs are associated with predisposition to chronic hepatitis C in Russian population. 24594345

2014

dbSNP: rs15895
rs15895
CUI: C0011311
Disease: Dengue Fever
Dengue Fever
0.010 GeneticVariation BEFREE Polymorphisms in the OAS1 (rs1131454 and rs10774671), OAS3 (rs2285932 and rs2072136) and OAS2 (rs15895 and rs1732778) genes were studied using PCR followed by restriction fragment length polymorphism methods in 109 patients hospitalized for dengue (DEN) and 105 healthy controls (HCs) who have no documented evidence of symptomatic dengue. 23337612

2013

dbSNP: rs739901
rs739901
CUI: C0014038
Disease: Encephalitis
Encephalitis
0.010 GeneticVariation BEFREE In EV71-infected patients, the CA genotype distribution (P=0.007), A allele frequency (OR 1.32,95% CI 1.0-1.7, P=0.034) and CA+AA carriage frequency (P=0.003) of OAS2 rs739901 5'-flanking were obviously elevated as compared with controls, but there were no statistically significant differences between mild cases and encephalitis cases. 30128873

2018