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SNP information rs17810546

RS17810546

Normal allele: AA

Common genetic variant in type 1 diabetes and celiac disease.

Polymorphism rs17810546 is related to topics like this:

Type 1 diabetes is it genetic

Our latest inclusion in the health report is the Type 1 Diabetes Genetic Risk Score, aimed at...


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.

  26097239   Brief report: Association of CCR1, KLRC4, IL12A-AS1, STAT4 and ERAP1 with Behçet's disease in Iranians.

  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.

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