Normal allele: AA
Common genetic variant in type 1 diabetes and celiac disease.
Polymorphism rs17810546 is related to topics like this:
Research and publications:
18311140 Newly identified genetic risk variants for celiac disease related to the immune response.
19073967 Shared and distinct genetic variants in type 1 diabetes and celiac disease
19458352 Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.
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.
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.
31726085 Celiac disease associated SNP rs17810546 is located in a gene silencing region.