rs2275913, IL17A

N. diseases: 105
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.
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.050 1.000 5 2008 2014
Asthma
CUI: C0004096
Disease: Asthma
1536 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.060 1.000 6 2010 2018
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.020 1.000 2 2010 2018
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.020 1.000 2 2010 2018
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2011 2011
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2011 2011
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.100 0.857 14 2012 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.100 0.857 14 2012 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2012 2012
Duodenal Diseases
CUI: C0013289
Disease: Duodenal Diseases
2 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2012 2012
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2012 2012
Mucosal atrophy
CUI: C2242595
Disease: Mucosal atrophy
5 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2012 2012
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2012 2012
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.050 0.600 5 2013 2017
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.030 1.000 3 2013 2017
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.020 1.000 2 2013 2016
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2013 2013
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2013 2013
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1 2013 2013
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2013 2013
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2013 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2013 2013
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2013 2013
Periodontal Diseases
CUI: C0031090
Disease: Periodontal Diseases
22 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2013 2013
Primary antiphospholipid syndrome
CUI: C0409980
Disease: Primary antiphospholipid syndrome
1 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2013 2013