rs2276886, CXCL9

N. diseases: 3
Disease: Graves Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.010 GeneticVariation BEFREE The MIG rs2276886 AG genotype was less frequent in patients with intractable GD (p = 0.0051). 27245471 2016