SNP information rs2066842

Research and publications:

  16008671   Association of CARD15 polymorphisms with atopy-related traits in a population-based cohort of Caucasian adults.

  16600026   Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathway

  17327408   Prognostic significance of host immune gene polymorphisms in follicular lymphoma survival

  18507017   Gene polymorphisms of the NOD-2/CARD-15 gene and the risk of gastric cancer in Germany.

  18633131   Host immune gene polymorphisms in combination with clinical and demographic factors predict late survival in diffuse large B-cell lymphoma patients in the pre-rituximab era

  18715515   Lack of evidence linking primary sclerosing cholangitis and primary biliary cirrhosis with Crohn's disease risk alleles in Polish patients.

  20230816   Association of c.802C>T polymorphism of NOD2/CARD15 gene with the chronic gastritis and predisposition to cancer in H. pylori infected patients.

  20595247   Polymorphisms of innate pattern recognition receptors, response to interferon-beta and development of neutralizing antibodies in multiple sclerosis patients.

  20698950   NOD2-C2 - a novel NOD2 isoform activating NF-kappaB in a muramyl dipeptide-independent manner.

  21304977   An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.

  21625457   Variation in NOD2 augments Th2- and Th17 responses to myelin basic protein in multiple sclerosis.

  21734790   NOD2 and ATG16L1 polymorphisms influence monocyte response in Crohn's disease.

  21745515   Role of NOD1/CARD4 and NOD2/CARD15 gene polymorphisms in cancer etiology.

  22319155   Crohn's disease risk alleles at the NOD2 locus are maintained by natural selection on standing variation.

  22427729   Inherited variation in pattern recognition receptors and cancer: dangerous liaisons?

  22957492   Pathway analysis of a genome-wide association study of ileal Crohn's disease.

  23085276   NOD2 gene mutations are weakly associated with ulcerative colitis but not Crohn's disease in Indian patients with inflammatory bowel disease.

  23651603   P268S in NOD2 is associated with Parkinson's disease susceptibility in a Chinese population.

  24033266   A systematic approach to assessing the clinical significance of genetic variants.

  24145928   Ethnicity differences in genetic susceptibility to ulcerative colitis: a comparison of Indian asians and white northern Europeans.

  26438151   The common NOD2/CARD15 variant P268S in patients with non-infectious uveitis: a cohort study.

  26643661   Preliminary evaluation of exome sequencing to identify genetic markers of susceptibility to tuberculosis disease.

  27128681   Genetic Variation in Autophagy-Related Genes Influences the Risk and Phenotype of Buruli Ulcer.

  27207565   Toxoplasma gondii exposure may modulate the influence of TLR2 genetic variation on bipolar disorder: a gene-environment interaction study.

  27404661   Polymorphisms in the mannose-binding lectin gene are associated with defective functional activity of mannose-binding lectin in patients with Crohn's disease.

  28822116   Interactions Between Variation in Candidate Genes and Environmental Factors in the Etiology of Schizophrenia and Bipolar Disorder: a Systematic Review.

  30061834   Impact of NOD2 variants on the outcome of treatment with Trichuris suis ova in Crohn's disease.

  32637927   Blau Syndrome and Early-Onset Sarcoidosis: A Six Case Series and Review of the Literature.

  34667597   Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy.