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.
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
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
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 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
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
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
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2019 2019
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
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
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
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
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