In VKH disease patients, there was an increased frequency of the CCL5/rs9355610 A allele (P = 0.029, OR = 0.805, and 95% CI = 0.662–0.979) and CXCL8/rs2227543 CT genotype (P = 0.016, OR = 0.72, and 95% CI = 0.552–0.940). The gene discussed is CXCL8; the disease is Vogt-Koyanagi-Harada disease.