rs8193036, IL17A

N. diseases: 21
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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.030 1.000 3 2015 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.030 0.333 3 2015 2019
Asthma
CUI: C0004096
Disease: Asthma
1536 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.020 1.000 2 2009 2016
Anthracosis
CUI: C0003165
Disease: Anthracosis
37 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2015 2015
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2012 2012
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2015 2015
Gastrointestinal Diseases
CUI: C0017178
Disease: Gastrointestinal Diseases
14 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2015 2015
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2014 2014
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2015 2015
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2013 2013
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2019 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2016 2016
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2015 2015
Obesity
CUI: C0028754
Disease: Obesity
1111 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2015 2015
Osteitis
CUI: C0029400
Disease: Osteitis
6 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2017 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2013 2013
Respiratory Distress Syndrome, Adult
CUI: C0035222
Disease: Respiratory Distress Syndrome, Adult
60 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2019 2019
Restless Legs Syndrome
CUI: C0035258
Disease: Restless Legs Syndrome
72 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2014 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2016 2016
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1 2016 2016
Uveitis, Intermediate
CUI: C0042166
Disease: Uveitis, Intermediate
10 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 0.010 1.000 1 2015 2015