rs7574865, STAT4

N. diseases: 59
Disease: Uveomeningoencephalitic Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Uveomeningoencephalitic Syndrome
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
0.010 GeneticVariation BEFREE Our results suggest that TT genotype of rs7574865 may be a susceptible factor for VKH syndrome in a Chinese Han population, and that GG genotype of this SNP may confer susceptibility in male BD patients. 20438790 2010