rs3761548, FOXP3

N. diseases: 42
Disease: Vitiligo ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Vitiligo
CUI: C0042900
Disease: Vitiligo
0.020 GeneticVariation BEFREE Significantly increased vitiligo risk was associated with the rs2232365 GG [odds ratio (OR) 1·68, 95% confidence interval (CI) 1·17-2·39, P = 0·004] and rs3761548 AA (OR 1·82, 95% CI 1·10-3·01, P = 0·033) genotypes compared with the rs2232365 AA and rs3761548 CC genotypes. 23582052 2013
Vitiligo
CUI: C0042900
Disease: Vitiligo
0.020 GeneticVariation BEFREE The rs3761548 of FOXP3 gene in our population may be associated with susceptibility to vitiligo because of altered expression. 23498308 2013