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.
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
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2015 2015
Thrombocytopenia due to platelet alloimmunization
CUI: C0272286
Disease: Thrombocytopenia due to platelet alloimmunization
7 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2013 2013
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.623 0.600 16 28507775 intron variant T/C snv 0.43 0.010 1.000 1 2016 2016