Variant: rs117633859 

    present in Gene: C1orf141;IL23R
    present in Chromosome: 1
    Position on Chromosome: 67162145
    Alleles of this Variant: A/G

rs117633859 in C1orf141;IL23R gene and Uveomeningoencephalitic Syndrome PMID 25108386 2014 We identified three loci associated with VKH syndrome susceptibility (IL23R-C1orf141, rs117633859, P(combined) = 3.42 × 10(-21), odds ratio (OR) = 1.82; ADO-ZNF365-EGR2, rs442309, P(combined) = 2.97 × 10(-11), OR = 1.37; and HLA-DRB1/DQA1, rs3021304, P(combined) = 1.26 × 10(-118), OR = 2.97).