{{Rsnum
|rsid=755622
|Gene=MIF
|Chromosome=22
|position=23894205
|Orientation=minus
|GMAF=0.2723
|Gene_s=NUBPL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{PMID Auto
|PMID=19941661
|Title=A MIF haplotype is associated with the outcome of patients with severe sepsis: a case control study
|OA=1
}}
{{PMID Auto
|PMID=20388640
|Title=Predictors of response to intra-articular steroid injection in psoriatic arthritis
}}
{{PMID Auto
|PMID=20439102
|Title=Analysis of MIF, FCGR2A and FCGR3A gene polymorphisms with susceptibility to pulmonary tuberculosis in Moroccan population
}}
{{PMID Auto
|PMID=20447688
|Title=The MIF -173G/C polymorphism and risk of childhood acute lymphoblastic leukemia in a Chinese population
}}
{{PMID Auto
|PMID=20471506
|Title=Polymorphisms in the macrophage migration inhibitory factor gene and bone loss in postmenopausal women
|OA=1
}}

{{PMID Auto
|PMID=22127710
|Title=Dual effect of the macrophage migration inhibitory factor gene on the development and severity of human systemic lupus erythematosus
|OA=1
}}

{{PMID Auto
|PMID=22568453
|Title=Association of CASP3 polymorphism with hematologic toxicity in advanced NSCLC patients treated with platinum-based chemotherapy
}}
{{PMID Auto
|PMID=16380915
|Title=Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4.
|OA=1
}}

{{PMID Auto
|PMID=16846490
|Title=Lemierre's syndrome and genetic polymorphisms: a case report.
|OA=1
}}

{{PMID Auto
|PMID=17585860
|Title=Macrophage migration inhibitory factor in acute lung injury: expression, biomarker, and associations.
|OA=1
}}

{{PMID Auto
|PMID=18242614
|Title=Macrophage migration inhibitory factor (MIF) and risk for coronary heart disease: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.
}}

{{PMID Auto
|PMID=18466472
|Title=Constructing gene association networks for rheumatoid arthritis using the backward genotype-trait association (BGTA) algorithm.
|OA=1
}}

{{PMID Auto
|PMID=18466513
|Title=Evaluating gene x gene and gene x smoking interaction in rheumatoid arthritis using candidate genes in GAW15.
|OA=1
}}

{{PMID Auto
|PMID=19167373
|Title=The macrophage migration inhibitory factor (MIF) gene polymorphism in Czech and Russian patients with myocardial infarction.
}}

{{PMID Auto
|PMID=20169173
|Title=Macrophage migration inhibitory factor: critical role in obesity, insulin resistance, and associated comorbidities.
|OA=1
}}

{{PMID Auto
|PMID=20811626
|Title=Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.
|OA=1
}}

{{PMID Auto
|PMID=21553324
|Title=Polymorphisms of the MDR1 and MIF genes in children with nephrotic syndrome.
}}

{{PMID Auto
|PMID=22417159
|Title=DNA sequence variation and regulation of genes involved in pathogenesis of pulmonary tuberculosis.
}}

{{PMID Auto
|PMID=23402792
|Title=Macrophage migration inhibitory factor (MIF): genetic evidence for participation in early onset and early stage rheumatoid arthritis
|OA=1
}}

{{PMID Auto
|PMID=24151396
|Title=Macrophage migration inhibitory factor gene polymorphisms in inflammatory bowel disease: An association study in New Zealand Caucasians and meta-analysis
|OA=1
}}

{{PMID Auto
|PMID=24160187
|Title=Meta-analysis confirms association between TNFA-G238A variant and JIA, and between PTPN22-C1858T variant and oligoarticular, RF-polyarticular and RF-positive polyarticular JIA
|OA=1
}}

{{PMID Auto
|PMID=24194192
|Title=MIF gene polymorphisms confer susceptibility to Vogt-Koyanagi-Harada syndrome in a Han Chinese population
}}

{{PMID Auto
|PMID=22820623
|Title=Association of MIF-173G/C and MBL2 codon 54 gene polymorphisms with rheumatoid arthritis: a meta-analysis.
}}

{{PMID Auto
|PMID=22939113
|Title=Association of macrophage migration inhibitory factor gene polymorphisms with Behcet's disease in a Han Chinese population.
}}

{{PMID Auto
|PMID=24951298
|Title=Macrophage migration inhibitory factor (MIF) -173 polymorphism is associated with clinical erythema nodosum in Löfgren's syndrome
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}