Disease: Severe myopia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Severe myopia
CUI: C0271183
Disease: Severe myopia
0.010 GeneticVariation BEFREE The reduced frequency of the heterozygote rs5751876 genotype in subjects suggests a possible association of A(2A)R with high myopia in a Chinese population. 22740769 2011