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.
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
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.020 0.500 2 2015 2016
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.030 1.000 3 2014 2019
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.020 1.000 2 2015 2015
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.020 1.000 2 2015 2015
Immune thrombocytopenic purpura
CUI: C0398650
Disease: Immune thrombocytopenic purpura
35 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.020 1.000 2 2013 2016
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.020 1.000 2 2016 2016
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.020 1.000 2 2015 2015
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.020 1.000 2 2015 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.020 1.000 2 2016 2017
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
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