Normal allele: AA
The JAK2 rs10758669 variant increases the risk of Crohn's disease: alteration of the intestinal barrier as one mechanism of action.
Polymorphism rs10758669 is related to topics like this:
Research and publications:
18006699 Host genetic variation contributes to phenotypic diversity in myeloproliferative disorders.
19287382 JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms.
20228799 Genome-wide association identifies multiple ulcerative colitis susceptibility loci.
20805105 Synthetic associations in the context of genome-wide association scan signals
21852963 Pervasive sharing of genetic effects in autoimmune disease.
22190364 Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
22359581 Th17-related genes and celiac disease susceptibility.
23028907 Limited evidence for parent-of-origin effects in inflammatory bowel disease associated loci.
24244878 Fibrogenesis and fibrosis in inflammatory bowel diseases: Good and bad side of same coin?
25133031 Genetic update on inflammatory factors in ulcerative colitis: Review of the current literature.
27156530 Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility.
27668286 Characterization of candidate genes in inflammatory bowel disease-associated risk loci.
18587394 Genome-wide association identifies more than 30 different susceptibility loci for Crohn's disease.
20570966 Nonsecretory fucosyltransferase 2 (FUT2) status is associated with Crohn's disease.
21730793 The influence of risk alleles for Crohn's disease and smoking on the location of the disease.
23300620 Genotype/phenotype analysis of 53 genetic polymorphisms associated with Crohn's disease.
27303667 Genetic influences on the development of fibrosis in Crohn's disease.