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.
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
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
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
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
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2013 2013
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
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2014 2014
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2014 2014
Malignant neoplasm of gastrointestinal tract
55 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2014 2014
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2014 2014
Osteoporosis, Postmenopausal
CUI: C0029458
Disease: Osteoporosis, Postmenopausal
38 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2014 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.020 0.500 2 2014 2015
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2015 2015