IL3, interleukin 3, 3562

N. diseases: 211; N. variants: 3
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs40401
rs40401 		0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.040 1.000 4 2004 2014
dbSNP: rs40401
rs40401 		0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.020 1.000 2 2009 2010
dbSNP: rs2073506
rs2073506 		0.925 0.200 5 132059045 upstream gene variant C/A;G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs2073506
rs2073506 		0.925 0.200 5 132059045 upstream gene variant C/A;G;T snv
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs2073506
rs2073506 		0.925 0.200 5 132059045 upstream gene variant C/A;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs31480
rs31480 		1.000 0.120 5 132060639 upstream gene variant C/G;T snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs40401
rs40401 		0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33
CUI: C2751898
Disease: Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Fibrillation, Paroxysmal Familial, 1 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs40401
rs40401 		0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33
CUI: C0861155
Disease: Rhinoconjunctivitis
Rhinoconjunctivitis 		Eye Diseases 0.010 1.000 1 2013 2013
dbSNP: rs40401
rs40401 		0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs40401
rs40401 		0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs40401
rs40401 		0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33
CUI: C0024530
Disease: Malaria
Malaria 		Infections 0.010 1.000 1 2011 2011
dbSNP: rs40401
rs40401 		0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 < 0.001 1 2016 2016