Normal allele: AA
Common genetic variant in type 1 diabetes and celiac disease.
Polymorphism rs17810546 is related to topics like this:
Research and publications:
18311140 Newly identified genetic risk variants for celiac disease related to the immune response.
18713140 Translational mini-review series on the immunogenetics of gut disease: immunogenetics of coeliac disease.
18853133 Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes.
19073967 Shared and distinct genetic variants in type 1 diabetes and celiac disease
19458352 Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.
19468064 Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions.
19648293 Replication of celiac disease UK genome-wide association study results in a US population.
20190752 Multiple common variants for celiac disease influencing immune gene expression.
20560212 Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection.
20647273 Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis.
20854658 Overlapping genetic susceptibility variants between three autoimmune disorders: rheumatoid arthritis, type 1 diabetes and coeliac disease.
21606320 Genetic associations with sporadic neuroendocrine tumor risk.
21760890 Potential celiac patients: a model of celiac disease pathogenesis.
21826374 Selective IgA deficiency in autoimmune diseases.
22087237 Improving the estimation of celiac disease sibling risk by non-HLA genes.
22174698 A comprehensive analysis of shared loci between systemic lupus erythematosus (SLE) and sixteen autoimmune diseases reveals limited genetic overlap.
25799145 Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behçet disease.
27417569 Systematic review: genetic biomarkers associated with anti-TNF treatment response in inflammatory bowel diseases.
27548383 Genetic Analysis with the Immunochip Platform in Behçet Disease. Identification of Residues Associated in the HLA Class I Region and New Susceptibility Loci.
31726085 Celiac disease associated SNP rs17810546 is located in a gene silencing region.
33216288 A First Step for the Molecular Characterization of Neurological Involvement of Behçet Syndrome: an Italian Pivotal Study.