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: 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: C0017638
Disease: Glioma
Glioma 		0.010 < 0.001 1 2016 2016
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.010 < 0.001 1 2015 2015
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis 		0.010 < 0.001 1 2013 2013
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.010 < 0.001 1 2019 2019
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0017638
Disease: Glioma
Glioma 		0.010 < 0.001 1 2016 2016
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		0.010 < 0.001 1 2013 2013
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.010 < 0.001 1 2015 2015
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0011206
Disease: Delirium
Delirium 		0.010 < 0.001 1 2011 2011
dbSNP: rs780209935
rs780209935
CXCL8
1.000 0.040 4 73742000 stop gained G/A snv 8.0E-06
CUI: C0679408
Disease: Lesion of stomach
Lesion of stomach 		0.010 < 0.001 1 2013 2013
dbSNP: rs2227532
rs2227532
CXCL8
0.882 0.120 4 73739815 upstream gene variant T/C snv 2.9E-02
CUI: C0031099
Disease: Periodontitis
Periodontitis 		0.020 0.500 2 2015 2017
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0031099
Disease: Periodontitis
Periodontitis 		0.020 0.500 2 2015 2017
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.040 0.750 4 2014 2020
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.050 0.800 5 2010 2019
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.050 0.800 5 2010 2019
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.040 1.000 4 2012 2018
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.040 1.000 4 2012 2018
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.040 1.000 4 2015 2019
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: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.020 1.000 2 2019 2019
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		0.020 1.000 2 2013 2019
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0271084
Disease: Exudative age-related macular degeneration
Exudative age-related macular degeneration 		0.020 1.000 2 2015 2016
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.020 1.000 2 2014 2018
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.020 1.000 2 2019 2019
dbSNP: rs1126647
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2016 2016