Normal allele: AA
Polymorphism rs2076756 is related to topics like this:
Research and publications:
17684544 Systematic association mapping identifies NELL1 as a novel IBD disease gene.
18758464 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.
19408013 Strategies and issues in the detection of pathway enrichment in genome-wide association studies
19434077 Detecting gene-gene interactions that underlie human diseases.
20505004 On safari to Random Jungle: a fast implementation of Random Forests for high-dimensional data.
20805105 Synthetic associations in the context of genome-wide association scan signals
21333900 The role of genetics in IBS
21427131 Improved Crohn's disease risk prediction using a multilocus approach.
21745515 Role of NOD1/CARD4 and NOD2/CARD15 gene polymorphisms in cancer etiology.
22127647 A novel bayesian graphical model for genome-wide multi-SNP association mapping.
22242114 The role of osteopontin haplotypes (OPN/SPP1) in susceptibility to Crohn's disease.
22412388 Genome-wide scanning of Crohn's disease of Ashkenazi Jews suggests new susceptibility loci.
22770979 Presence of multiple independent effects in risk loci of common complex human diseases.
23365659 IRGM variants and susceptibility to inflammatory bowel disease in the German population.
25664710 Genetic determinants associated with early age of diagnosis of IBD.
26833331 Retrospective Binary-Trait Association Test Elucidates Genetic Architecture of Crohn Disease.
27153677 Assessing statistical significance in multivariable genome wide association analysis.
27303667 Genetic influences on the development of fibrosis in Crohn's disease.
32045400 Clinical and genetic factors associated with complications after Crohn's ileocolectomy.