Normal allele: CC
Associated with type 1 diabetes mellitus, organ-specific autoimmune diseases including Graves' disease.
Polymorphism rs1990760 is related to topics like this:
Research and publications:
17554260 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
17940599 Assembly of inflammation-related genes for pathway-focused genetic analysis.
18071670 The association between the IFIH1 locus and type 1 diabetes.
18285833 IFIH1-GCA-KCNH7 locus: influence on multiple sclerosis risk.
18647951 A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3.
18840781 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.
18987646 The expanding genetic overlap between multiple sclerosis and type I diabetes.
19073967 Shared and distinct genetic variants in type 1 diabetes and celiac disease
19264985 Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes.
19732865 A generalized family-based association test for dichotomous traits.
19951419 Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis.
19956101 Overview of the Rapid Response data
20203524 Genetic susceptibility to type 2 diabetes is associated with reduced prostate cancer risk
20392289 Genetic associations in type I interferon related pathways with autoimmunity.
20587799 Genetics of type 1 diabetes: what next?
20644636 Study of transcriptional effects in Cis at the IFIH1 locus.
20668468 Carriers of rare missense variants in IFIH1 are protected from psoriasis.
20694011 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.
20805105 Synthetic associations in the context of genome-wide association scan signals
20844740 Reduced expression of IFIH1 is protective for type 1 diabetes.
20933377 Recent findings on genetics of systemic autoimmune diseases.
21270831 Association between type 1 diabetes and GWAS SNPs in the southeast US Caucasian population.
21826374 Selective IgA deficiency in autoimmune diseases.
21829393 Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.
21852963 Pervasive sharing of genetic effects in autoimmune disease.
21873553 Genetic analysis of adult-onset autoimmune diabetes.
21980299 A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.
22046141 Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus.
22187373 Why are C-section deliveries linked to childhood type 1 diabetes?
22242199 Genetic factors of autoimmune thyroid diseases in Japanese.
22536486 Lupus nephritis: an overview of recent findings.
22640752 The genetics of lupus: a functional perspective.
22654555 Genetic basis of Graves' disease.
22770979 Presence of multiple independent effects in risk loci of common complex human diseases.
23036011 Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.
23804261 From markers to molecular mechanisms: type 1 diabetes in the post-GWAS era.
24653663 Systemic Lupus Erythematosus: Old and New Susceptibility Genes versus Clinical Manifestations.
24661571 Laying a strong foundation for Manhattan—“laying a functional foundation for the post-GWAS era.”
25034154 Clinical perspectives on lupus genetics: advances and opportunities.
25042601 Association analysis of PTPN22, CTLA4 and IFIH1 genes with type 1 diabetes in Colombian families.
26324017 Immunogenetics of systemic lupus erythematosus: A comprehensive review.
26613086 Polymorphisms Associated with Age at Onset in Patients with Moderate-to-Severe Plaque Psoriasis.
27047537 Using Incomplete Trios to Boost Confidence in Family Based Association Studies.
27810495 Psoriasis risk SNPs and their association with HIV-1 control.
29070082 Sex influences eQTL effects in SLE and genetic polymorphisms associated with Sjögren's syndrome.
30327483 Phenome-wide association studies across large population cohorts support drug target validation.