Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011 2018
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease BEFREE In addition, the significant gene-gene interactions among IL-4 -C33T, IL-13 R130Q, IL-4Ralpha I75V, IL-4Ralpha Q576R, STAT6 C2892T, and CD14 -C159T may increase an individual's susceptibility to asthma and contribute to the pathogenesis of asthma. 20394509 2010
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease BEFREE Direct sequencing analysis revealed that the 13 GT repeat allelic variation in noncoding exon 1 of the STAT6 gene appeared more frequently in 91 patients with asthma or rheumatoid arthritis than the 15 GT repeat variation, which is the dominant phenotype in healthy controls. 19949830 2010
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease BEFREE We have studied the association of polymorphism rs4795405 in ORMDL3, rs324011 in STAT6 as well as rs8113232 and rs3786989 in TBXA2R with asthma risk, various asthma phenotypes and asthma-related symptoms. 22017802 2012
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease BEFREE Home dampness combined with each one of the genes STAT6, IL13 and ADRB2 could raise the asthma risk. 22355322 2012
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease BEFREE An asthma-associated genetic variant of STAT6 predicts low burden of ascaris worm infestation. 14735150 2004
CUI: C0004096
Disease: Asthma
Asthma
0.400 GeneticVariation disease GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.400 GeneticVariation disease BEFREE In Egyptian children, the IL-4Rα and the STAT6 polymorphism may play a role in susceptibility to AD. 24742632 2014
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.400 GeneticVariation disease BEFREE We used data from the Han Chinese in Beijing genome panel of International HapMap Project and the Taiwan Children Health Study cohort to investigate the association of STAT6 genetic variants and childhood AD risks. 26048407 2015
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.400 GeneticVariation disease BEFREE Moreover, there was a significant association between genotype and allele frequencies of the STAT6 (G2946A) polymorphism in the non-AD (P < 0.05) and AD (P < 0.01) groups. 27018548 2016
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.400 GeneticVariation disease BEFREE We undertook an association study between these variants of the STAT6 gene and allergic diseases, including atopic dermatitis, bronchial asthma, and food-related anaphylaxis in a Japanese population. 12759487 2003
CUI: C0018922
Disease: hemangiopericytoma
hemangiopericytoma
0.390 GeneticVariation disease BEFREE Clinicopathological data, including yearly follow-ups, are required for meningeal SFTs/HPCs to define the correlation of variants of NAB2-STAT6 fusion gene. 27271270 2016
CUI: C0018922
Disease: hemangiopericytoma
hemangiopericytoma
0.390 GeneticVariation disease BEFREE The 2016 central nervous system (CNS) World Health Organisation (WHO) Update has merged the entities of meningeal solitary fibrous tumor (SFT) and hemangiopericytoma (HPC) into a single entity based on the presence of the nerve growth factor 1A (NGFI-A) binding protein 2 (NAB2)- signal transducer and activator of transcription 6 (STAT6) gene fusion in these tumors. 30233017 2019
CUI: C0013595
Disease: Eczema
Eczema
0.200 GeneticVariation disease BEFREE Moreover, there was a significant association between genotype and allele frequencies of the STAT6 (G2946A) polymorphism in the non-AD (P < 0.05) and AD (P < 0.01) groups. 27018548 2016
CUI: C0013595
Disease: Eczema
Eczema
0.200 GeneticVariation disease BEFREE We used data from the Han Chinese in Beijing genome panel of International HapMap Project and the Taiwan Children Health Study cohort to investigate the association of STAT6 genetic variants and childhood AD risks. 26048407 2015
CUI: C0013595
Disease: Eczema
Eczema
0.200 GeneticVariation disease GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0013595
Disease: Eczema
Eczema
0.200 GeneticVariation disease BEFREE We undertook an association study between these variants of the STAT6 gene and allergic diseases, including atopic dermatitis, bronchial asthma, and food-related anaphylaxis in a Japanese population. 12759487 2003
CUI: C0013595
Disease: Eczema
Eczema
0.200 GeneticVariation disease BEFREE Our study adds to the current knowledge of genetic susceptibility by demonstrating for the first time an interactive effect between SNPs in IL13 (rs20541) and STAT6 (rs1059513) on the occurrence of eczema in two independent samples. 23815671 2013
CUI: C0013595
Disease: Eczema
Eczema
0.200 GeneticVariation disease BEFREE In Egyptian children, the IL-4Rα and the STAT6 polymorphism may play a role in susceptibility to AD. 24742632 2014
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.170 GeneticVariation disease BEFREE Here we report genome-wide significant associations at four additional loci; c11orf30 and STAT6, which have been previously associated with both atopic and autoimmune diseases, and two EoE-specific loci, ANKRD27 that regulates the trafficking of melanogenic enzymes to epidermal melanocytes and CAPN14, that encodes a calpain whose expression is highly enriched in the oesophagus. 25407941 2014
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.170 GeneticVariation disease GWASCAT GWAS identifies four novel eosinophilic esophagitis loci. 25407941 2014
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.170 GeneticVariation disease BEFREE Common variants in CYP2C19 and STAT6 associate with a PPI-nonresponsive EoE outcome of PPI therapy for esophageal eosinophilia suggesting that response rates may be improved by adopting a genotype-guided approach to PPI dosing. 31490856 2019
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.110 GeneticVariation disease GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.110 GeneticVariation disease BEFREE The MDR analysis showed that GT repeats, C258T and T710C of STAT6 polymorphisms interacted together in leading to susceptibility to childhood asthma among Chinese people. 22365404 2011
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.110 GeneticVariation disease GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019