rs9355610, LOC105378120

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
0.850 GeneticVariation BEFREE This study was designed to unveil the association of GPR174 rs3827440, PTPN22 rs3789604, and RNASET2 rs9355610 with the onset of liver damage (LD) among the Graves' disease (GD) patients. 28568286 2018
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.850 GeneticVariation BEFREE Association analysis revealed both rs6832151 located in 4p14 (odds ratio (OR) = 1.27, P <sub>Allelic</sub>  = 1.48 × 10<sup>-9</sup>) and rs9355610 located in 6q27 (OR = 1.10, P <sub>Allelic</sub>  = 1.04 × 10<sup>-2</sup>) was associated with GD susceptibility. 28521825 2017
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.850 GeneticVariation BEFREE Our results suggest that the rs9355610 tag SNP of RNASET2 gene is positively associated with susceptibility to GD in the Chinese Han population. 25928629 2015
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.850 GeneticVariation BEFREE The replication of the association of the rs9355610 within 6p27 with Graves' disease. 24001206 2013
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.850 GeneticVariation BEFREE Our findings are the first to show that rs6832151 and possibly rs9355610 contribute to GD pathogenesis also in Caucasians. 22489947 2012
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.850 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.850 GeneticVariation GWASCAT A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011