rs2276886, CXCL9

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autoimmune thyroid disease
CUI: C0178468
Disease: Autoimmune thyroid disease
0.010 GeneticVariation BEFREE Recently, the single nucleotide polymorphism (SNP) rs2276886 associated with the <i>CXCL9</i> gene was identified as associated with autoimmune thyroid disease susceptibility in Japanese populations. 31750736 2019
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
0.010 GeneticVariation BEFREE In this study, we first reported that the polymorphisms in IL8, RANTES and MIG genes are associated with the development of AITD, and that the MIG rs2276886 AG genotype is associated with the intractability of GD. 27245471 2016
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
0.010 GeneticVariation BEFREE To clarify the association between functional polymorphisms in genes encoding some chemokines and the pathogenesis of Autoimmune thyroid disease (AITD), we genotyped IL8 -251T/A, Regulated upon Activation, Normal T cell Expressed and presumably Secreted (RANTES) - 403G/A, -28C/G, MIG rs2276886G/A, IP10 -1596C/T, Monocyte Chemoattractant Protein1 (MCP1) - 2518G/A and IL16 -295T/C polymorphisms. 27245471 2016
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