rs225014, DIO2

N. diseases: 22
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
0.030 GeneticVariation BEFREE Seven SNPs in the DIO2 gene - rs225014 (Thr92Ala), rs12885300, rs2267872, rs225011, rs224995, rs225015, and rs2267873 - were studied to assess their association with GD and GO. 30574458 2018
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.030 GeneticVariation BEFREE Type 2 deiodinase Thr92Ala polymorphism impact on clinical course and myocardial remodeling in patients with Graves' disease. 19684474 2009
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.030 GeneticVariation BEFREE This suggests that the Thr92Ala variant of the DIO2 gene is associated or may be in linkage disequilibrium with a functional DIO2 polymorphism which involves in the development of GD in a Russian population. 15542398 2004