rs16944, IL1B

N. diseases: 91
Source: BEFREE ×
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 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
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
68 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
273 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
2145 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
995 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
28 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
50 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
cervical cancer
CUI: C4048328
Disease: cervical cancer
257 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2015 2019
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
266 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2015 2019
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
301 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
5 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.030 1.000 3 2014 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 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
769 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
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
178 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2010 2013
Dementia
CUI: C0497327
Disease: Dementia
165 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2010 2011
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2016 2019
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
290 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2016 2019
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
120 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.030 1.000 3 2015 2019