Normal allele: CC
Polymorphism rs917997 is related to topics like this:
Research and publications:
18311140 Newly identified genetic risk variants for celiac disease related to the immune response.
18587394 Genome-wide association identifies more than 30 different susceptibility loci for Crohn's disease.
19073967 Shared and distinct genetic variants in type 1 diabetes and celiac disease
19103669 Association study of the IL18RAP locus in three European populations with coeliac disease.
19648293 Replication of celiac disease UK genome-wide association study results in a US population.
19915574 Common variants at five new loci associated with early-onset inflammatory bowel disease.
20190752 Multiple common variants for celiac disease influencing immune gene expression.
20228799 Genome-wide association identifies multiple ulcerative colitis susceptibility loci.
20353565 Allelic variants of IL1R1 gene associate with severe hand osteoarthritis.
20570966 Nonsecretory fucosyltransferase 2 (FUT2) status is associated with Crohn's disease.
20587799 Genetics of type 1 diabetes: what next?
20805105 Synthetic associations in the context of genome-wide association scan signals
21150878 Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.
21629437 Genetics of interleukin 1 receptor-like 1 in immune and inflammatory diseases.
21760890 Potential celiac patients: a model of celiac disease pathogenesis.
21826374 Selective IgA deficiency in autoimmune diseases.
21852963 Pervasive sharing of genetic effects in autoimmune disease.
24621393 Genetic polymorphisms in the IL-18 gene and ulcerative colitis risk: a meta-analysis.
25980667 Pharmacogenetics of treatment response in psoriatic arthritis.
26229413 Genetic polymorphisms of interleukin-18 have different effects on susceptibility to Crohn's disease.
26566691 Polymorphisms of ST2-IL18R1-IL18RAP gene cluster: a new risk for autoimmune thyroid diseases.
27156530 Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility.
27536357 Genetic predisposition to Barrett's esophagus: lessons from early research.
27863251 Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.
31126849 Role of APOE and IL18RAP gene polymorphisms in cervical spondylotic myelopathy in Indian population.
31147177 IL18RAP polymorphisms and its plasma levels in patients with Lumbar disc degeneration.
33262486 Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters.