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.
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
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
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
Autoimmune liver disease
CUI: C0400936
Disease: Autoimmune liver disease
3 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1 2018 2018
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2016 2016
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
Cancer of Nasopharynx
CUI: C0238301
Disease: Cancer of Nasopharynx
12 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2016 2016
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
Candidiasis
CUI: C0006840
Disease: Candidiasis
8 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2015 2015
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
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2019 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2016 2016
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
3 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2013 2013
Childhood Acute Lymphoblastic Leukemia
261 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2017 2017
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2016 2016
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
14 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2015 2015
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2019 2019
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
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2016 2016
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2018 2018
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
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2018 2018
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2017 2017