rs1800896, IL19;IL10

N. diseases: 113
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.
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2007 2007
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2008 2010
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2008 2010
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2008 2010
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2010 2010
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2010 2010
Glioma
CUI: C0017638
Disease: Glioma
353 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2010 2010
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2007 2011
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2011 2011
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2012 2012
Candidemia
CUI: C0877445
Disease: Candidemia
11 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2012 2012
Heparin-induced thrombocytopenia
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
5 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2012 2012
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2013 2013
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2013 2013
Cervical Squamous Intraepithelial Neoplasia
CUI: C1332922
Disease: Cervical Squamous Intraepithelial Neoplasia
3 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2013 2013
Classical Hodgkin's Lymphoma
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
20 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2013 2013
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2013 2013
T-Cell Lymphoma
CUI: C0079772
Disease: T-Cell Lymphoma
24 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2013 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.040 0.750 4 2009 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 0.333 3 2012 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 0.333 3 2012 2014
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2009 2014
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2014 2014
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2014 2014
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
232 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2014 2014