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.
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
Keratoconus
CUI: C0022578
Disease: Keratoconus
83 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2008 2013
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2009 2009
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2009 2009
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
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
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
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.020 1.000 2 2010 2011
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
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2010 2010
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
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
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
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
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2011 2011
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 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
Seizures
CUI: C0036572
Disease: Seizures
553 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2012 2012
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2013 2013
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2013 2013
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2013 2013
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