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.
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.050 1.000 5 2014 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.040 1.000 4 2014 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.040 1.000 4 2014 2016
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.030 1.000 3 2014 2017
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.020 1.000 2 2014 2017
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
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
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
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.070 0.857 7 2015 2020
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.060 1.000 6 2015 2017
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.060 1.000 6 2015 2017
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.060 1.000 6 2015 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.050 1.000 5 2015 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.020 1.000 2 2015 2016
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
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.010 1.000 1 2015 2015
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 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
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
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
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