rs2227306, CXCL8

N. diseases: 21
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2015 2015
Arthritis, Gouty
CUI: C0003868
Disease: Arthritis, Gouty
2356 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1 2016 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2017 2017
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2019 2019
Cystic Fibrosis
CUI: C0010674
Disease: Cystic Fibrosis
704 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2016 2016
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2014 2014
Glioma
CUI: C0017638
Disease: Glioma
353 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1 2016 2016
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2009 2009
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2016 2016
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
63 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2011 2011
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2011 2011
Lichen Planus, Oral
CUI: C0206139
Disease: Lichen Planus, Oral
20 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2010 2010
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2015 2015
Lung diseases
CUI: C0024115
Disease: Lung diseases
50 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2016 2016
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2015 2015
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2019 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2014 2014
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2019 2019
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2016 2016
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2016 2016
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.677 0.680 4 73741338 intron variant C/T snv 0.31 0.010 1.000 1 2009 2009