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.
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
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
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
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
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
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
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
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2010 2010
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 neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2013 2013
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2013 2013
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
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
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
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
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016
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
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2015 2015
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
Osteoarthritis of hip
CUI: C0029410
Disease: Osteoarthritis of hip
121 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2011 2011
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
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016