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.
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
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
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
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
Post-Traumatic Stress Disorder
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
117 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2017 2017
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
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
65 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2018 2018
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2010 2018
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
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
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
Interleukin 1 Beta Measurement
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
149 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.700 1.000 1 2018 2018
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2018 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2018 2018
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
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2018 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2018 2018
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
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
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2015 2019