OR11H1 and Vogt-Koyanagi-Harada disease: Numerous studies have examined the association between HLA and VKH disease, therefore, we focused on the non‐HLA gene OR11H1 in the current study.[4, 23, 24, 25] The OR11H1 rare variant (a frequency less than 0.05) in Chr 22 rs71235604 (c.188T>C) was significantly associated with VKH disease (WES: P = 3.21 × 10−24, OR = 11.53; NGS: P = 9.29 × 10−7, OR = 1.73; Combined: P = 7.83 × 10−30, OR = 3.12) (Table 1).