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.
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
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2011 2011
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1 2012 2012
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
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 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
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
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
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
Fatigue
CUI: C0015672
Disease: Fatigue
67 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 0.500 2 2011 2012
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
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 0.500 2 2014 2016
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 0.500 2 2014 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.040 0.750 4 2010 2014
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.060 0.833 6 2006 2016
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
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2015 2019
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 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
176 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
297 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2016 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2016 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