Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs744166
rs744166
STAT3
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		A 0.870 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394

2008
dbSNP: rs744166
rs744166
STAT3
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.820 GeneticVariation GWASDB SNP (rs744166) within the STAT3 gene was associated to MS (p = 2.75 x 10(-10), OR 0.87, confidence interval 0.83-0.91). 20159113

2010
dbSNP: rs9891119
rs9891119
STAT3
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		A 0.810 GeneticVariation GWASDB We confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)). 23266558

2013
dbSNP: rs12942547
rs12942547
STAT3
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		A 0.800 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233

2012
dbSNP: rs2293152
rs2293152
STAT3
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.800 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011
dbSNP: rs9891119
rs9891119
STAT3
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.800 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs744166
rs744166
STAT3
CUI: C0004096
Disease: Asthma
Asthma 		0.700 GeneticVariation GWASDB Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. 21150878

2011