rs153109, IL27

N. diseases: 37
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 lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2018 2018
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2018 2018
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2014 2014
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2017 2017
Autoimmune thrombocytopenia
CUI: C0242584
Disease: Autoimmune thrombocytopenia
7 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2013 2013
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2014 2014
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2017 2017
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2016 2016
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2017 2017
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2018 2018
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2016 2016
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2015 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1 2016 2016
Coronary Stenosis
CUI: C0242231
Disease: Coronary Stenosis
20 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1 2016 2016
Cryptorchidism
CUI: C0010417
Disease: Cryptorchidism
80 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2016 2016
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2016 2016
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2019 2019
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2014 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2014 2014
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2016 2016
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2016 2016
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2016 2016
Precursor Cell Lymphoblastic Leukemia Lymphoma
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2018 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1 2015 2015