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.
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2017 2017
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2017 2017
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
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
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
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2016 2016
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2016 2016
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2015 2015
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
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2015 2015
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2017 2017
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
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
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2017 2017
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
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
Leprosy
CUI: C0023343
Disease: Leprosy
120 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2019 2019
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2016 2016
Lupus Erythematosus
CUI: C0409974
Disease: Lupus Erythematosus
44 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2016 2016
Lupus Erythematosus, Discoid
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
46 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2016 2016
Lupus Nephritis
CUI: C0024143
Disease: Lupus Nephritis
64 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1 2016 2016
Lupus Vulgaris
CUI: C0024131
Disease: Lupus Vulgaris
44 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2016 2016
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
Malignant neoplasm of gastrointestinal tract
CUI: C0685938
Disease: 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