rs11209026, IL23R

N. diseases: 46
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 rs11209026 SNP, which is the most strongly associated with Crohn's disease, was not associated with GD or GO in our data set. 18073300 2008