rs16944, IL1B

N. diseases: 92
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.
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2011 2011
Anthracosilicosis
CUI: C0003164
Disease: Anthracosilicosis
4 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2018 2018
Anxiety symptoms
CUI: C0860603
Disease: Anxiety symptoms
10 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2018 2018
Carpal Tunnel Syndrome
CUI: C0007286
Disease: Carpal Tunnel Syndrome
46 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2015 2015
CATARACT, ANTERIOR POLAR
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
27 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
CUI: C1302547
Disease: Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
14 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2015 2015
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2014 2014
Chronic osteomyelitis
CUI: C0008707
Disease: Chronic osteomyelitis
12 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2013 2013
Community acquired pneumonia
CUI: C0694549
Disease: Community acquired pneumonia
13 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016
Cytomegalovirus Infections
CUI: C0010823
Disease: Cytomegalovirus Infections
26 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2009 2009
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2009 2009
Diabetic peripheral neuropathy
CUI: C0740447
Disease: Diabetic peripheral neuropathy
16 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2012 2012
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2013 2013
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2013 2013
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2018 2018
Gastritis
CUI: C0017152
Disease: Gastritis
21 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016