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.
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
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
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
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
Silent myocardial ischemia
CUI: C0340291
Disease: Silent myocardial ischemia
4 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2015 2015
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2013 2013
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
Stress, Psychological
CUI: C0038443
Disease: Stress, Psychological
24 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016
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
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2016 2016
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
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
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
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
42 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2015 2015
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2014 2014
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2014 2014