rs4073, CXCL8

N. diseases: 64
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.
Acute focal bacterial nephritis
CUI: C3266959
Disease: Acute focal bacterial nephritis
5 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2011 2011
Acute periodontitis
CUI: C0001342
Disease: Acute periodontitis
49 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1 2013 2013
Acute pyelonephritis
CUI: C0520575
Disease: Acute pyelonephritis
10 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2011 2011
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2015 2015
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2014 2014
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1 2015 2015
Aggressive Periodontitis
CUI: C0031106
Disease: Aggressive Periodontitis
59 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1 2013 2013
Aggressive periodontitis, generalized
CUI: C1719495
Disease: Aggressive periodontitis, generalized
16 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2013 2013
Arthritis, Gouty
CUI: C0003868
Disease: Arthritis, Gouty
2356 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2016 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2017 2017
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2019 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2014 2014
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2017 2017
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2015 2015
CATARACT, ANTERIOR POLAR
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
27 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2016 2016
Central Diabetes Insipidus
CUI: C0687720
Disease: Central Diabetes Insipidus
21 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2014 2014
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2014 2014
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2011 2011
Clostridium difficile infection
CUI: C0343386
Disease: Clostridium difficile infection
10 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2014 2014
Community acquired pneumonia
CUI: C0694549
Disease: Community acquired pneumonia
13 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2016 2016
Completed Suicide
CUI: C0852733
Disease: Completed Suicide
33 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2018 2018
Cystic Fibrosis
CUI: C0010674
Disease: Cystic Fibrosis
704 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2016 2016
Delirium
CUI: C0011206
Disease: Delirium
7 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1 2011 2011
Glioma
CUI: C0017638
Disease: Glioma
353 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1 2016 2016
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
269 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1 2015 2015