Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2489188
rs2489188
TGFBR3
0.010 GeneticVariation BEFREE In this study, we analysed the potential association of the type III TGF-β receptor (TGFBR3) genetic variations (rs2489188 and rs1805110) in the Chinese Han population for patients with either Vogt-Koyanagi-Harada (VKH) disease or Behcet's disease (BD), two uveitis entities presumably mediated by Th17 cells. 22440163

2012