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.
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
Silent myocardial ischemia
CUI: C0340291
Disease: Silent myocardial ischemia
4 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2015 2015
Mesial temporal lobe epilepsy with hippocampal sclerosis
CUI: C4749367
Disease: Mesial temporal lobe epilepsy with hippocampal sclerosis
7 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2018 2018
Ocular Toxoplasmosis
CUI: C0040561
Disease: Ocular Toxoplasmosis
9 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
Ketosis
CUI: C0022638
Disease: Ketosis
11 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2011 2011
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
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
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
Osteomyelitis
CUI: C0029443
Disease: Osteomyelitis
14 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
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
Influenza
CUI: C0021400
Disease: Influenza
17 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2019 2019
Leishmaniasis, Cutaneous
CUI: C0023283
Disease: Leishmaniasis, Cutaneous
17 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Influenza A
CUI: C2062441
Disease: Influenza A
19 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2015 2015
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
Periodontal Diseases
CUI: C0031090
Disease: Periodontal Diseases
22 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 0.500 2 2014 2019
Recurrent aphthous ulcer
CUI: C2937365
Disease: Recurrent aphthous ulcer
22 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
Stress, Psychological
CUI: C0038443
Disease: Stress, Psychological
24 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
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
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2011 2011
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
42 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2015 2015
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
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2010 2010
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2013 2013