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.
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
Digestive System Neoplasms
CUI: C0012243
Disease: Digestive System Neoplasms
2 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2019 2019
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
Panuveitis
CUI: C0030343
Disease: Panuveitis
2 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2015 2015
Viral myocarditis
CUI: C0276138
Disease: Viral myocarditis
2 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2018 2018
Acute bronchiolitis
CUI: C0001311
Disease: Acute bronchiolitis
3 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2017 2017
Syphilis
CUI: C0039128
Disease: Syphilis
3 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2018 2018
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
Rheumatic Fever
CUI: C0035436
Disease: Rheumatic Fever
5 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2018 2018
Osteitis
CUI: C0029400
Disease: Osteitis
6 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.020 1.000 2 2017 2017
Appendicitis
CUI: C0003615
Disease: Appendicitis
10 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2020 2020
Chagas Disease
CUI: C0041234
Disease: Chagas Disease
10 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2017 2017
Uveitis, Intermediate
CUI: C0042166
Disease: Uveitis, Intermediate
10 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2015 2015
Left ventricular systolic dysfunction
CUI: C1277187
Disease: Left ventricular systolic dysfunction
11 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2017 2017
Post transplant diabetes mellitus
CUI: C1504532
Disease: Post transplant diabetes mellitus
11 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2015 2015
Gastrointestinal Diseases
CUI: C0017178
Disease: Gastrointestinal Diseases
14 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2015 2015
Influenza
CUI: C0021400
Disease: Influenza
17 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1 2019 2019
Leishmaniasis, Cutaneous
CUI: C0023283
Disease: Leishmaniasis, Cutaneous
17 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2019 2019
Influenza A
CUI: C2062441
Disease: Influenza A
19 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2019 2019
Rhinitis
CUI: C0035455
Disease: Rhinitis
20 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2018 2018
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
Spondylarthritis
CUI: C0949690
Disease: Spondylarthritis
23 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2018 2018
Active tuberculosis
CUI: C0151332
Disease: Active tuberculosis
25 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2017 2017
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
Necrotizing enterocolitis in fetus OR newborn
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
26 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1 2017 2017