Disease: Central Serous Chorioretinopathy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Central Serous Chorioretinopathy
CUI: C0730328
Disease: Central Serous Chorioretinopathy
0.010 GeneticVariation BEFREE Patients with CVH had a significantly higher frequency of the G allele of ARMS2 A69S (rs10490924) and the T allele of CFH (rs1329428), which are reported to be risk alleles for central serous chorioretinopathy (P = 0.006 and P = 0.032, respectively; multivariate regression analysis). 26745149 2016