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: rs1126647
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.010 1.000 1 2018 2018
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C3266959
Disease: Acute focal bacterial nephritis
Acute focal bacterial nephritis 		0.010 1.000 1 2011 2011
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: 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: C0520575
Disease: Acute pyelonephritis
Acute pyelonephritis 		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: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma 		0.010 1.000 1 2015 2015
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
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma 		0.010 1.000 1 2014 2014
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: 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: C1719495
Disease: Aggressive periodontitis, generalized
Aggressive periodontitis, generalized 		0.010 1.000 1 2013 2013
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: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		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: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2017 2017
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2017 2017
dbSNP: rs1126647
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/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: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		0.010 1.000 1 2019 2019
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		0.010 1.000 1 2019 2019
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2017 2017
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2015 2015
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
CATARACT, ANTERIOR POLAR 		0.010 1.000 1 2016 2016
dbSNP: rs4073
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0687720
Disease: Central Diabetes Insipidus
Central Diabetes Insipidus 		0.010 1.000 1 2014 2014
dbSNP: rs2227307
rs2227307
CXCL8
0.851 0.240 4 73740952 intron variant T/G snv 0.45
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma 		0.010 1.000 1 2014 2014