Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2227307
rs2227307
CXCL8
0.851 0.240 4 73740952 intron variant T/G snv 0.45
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis 		0.020 1.000 2 2016 2017
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2017 2017
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2019 2019
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
Liver and Intrahepatic Biliary Tract Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0024115
Disease: Lung diseases
Lung diseases 		0.010 1.000 1 2016 2016
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0206139
Disease: Lichen Planus, Oral
Lichen Planus, Oral 		0.010 1.000 1 2010 2010
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2014 2014
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		0.010 1.000 1 2011 2011
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		0.010 1.000 1 2019 2019
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis 		0.010 1.000 1 2011 2011
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver 		0.010 1.000 1 2015 2015
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2016 2016
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.010 < 0.001 1 2016 2016
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.010 1.000 1 2009 2009
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0017638
Disease: Glioma
Glioma 		0.010 < 0.001 1 2016 2016
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis 		0.010 1.000 1 2016 2016
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2016 2016
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.010 1.000 1 2014 2014
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies 		0.010 1.000 1 2009 2009
dbSNP: rs2227306
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		0.010 1.000 1 2016 2016
dbSNP: rs2227307
rs2227307
CXCL8
0.851 0.240 4 73740952 intron variant T/G snv 0.45
CUI: C0024115
Disease: Lung diseases
Lung diseases 		0.010 1.000 1 2016 2016
dbSNP: rs2227307
rs2227307
CXCL8
0.851 0.240 4 73740952 intron variant T/G snv 0.45
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis 		0.010 1.000 1 2011 2011
dbSNP: rs2227307
rs2227307
CXCL8
0.851 0.240 4 73740952 intron variant T/G snv 0.45
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma 		0.010 1.000 1 2014 2014