rs2294025, TG

N. diseases: 1
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
0.810 GeneticVariation BEFREE The fine mapping study of thyroglobulin identified two independent SNPs (rs2294025 and rs7005834) for GD susceptibility. 31700870 2019
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.810 GeneticVariation GWASCAT Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. 23612905 2013
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.810 GeneticVariation GWASDB Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. 23612905 2013