rs5522, NR3C2

N. diseases: 19
Disease: Chronic central serous chorioretinopathy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Chronic central serous chorioretinopathy
CUI: C0730314
Disease: Chronic central serous chorioretinopathy
0.010 GeneticVariation BEFREE Moreover, the GA haplotype of single-nucleotide polymorphisms rs2070951 and rs5522 in NR3C2 conferred risk for cCSC (odds ratio, 1.39; 95% CI, 1.15-1.68; P = .004), whereas the CA haplotype decreased risk for cCSC (odds ratio, 0.72; 95% CI, 0.60-0.87; P < .001). 28334414 2017