Normal allele: CC
Polymorphism rs3761959 is related to topics like this:
Research and publications:
17952073 Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.
19452015 Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome.
20453842 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.
22242199 Genetic factors of autoimmune thyroid diseases in Japanese.
22654555 Genetic basis of Graves' disease.
23094030 Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis.
25594855 FCRL3 gene polymorphisms confer autoimmunity risk for allergic rhinitis in a Chinese Han population.
27863461 Pooled genome-wide association reveals association upstream of FCRL3 with Graves' disease.
31341856 Single nucleotide polymorphisms of FCRL3 in Iranian patients with Behçet's disease.