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
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 0.667 3 2013 2017
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
African Burkitt's lymphoma
CUI: C0343640
Disease: African Burkitt's lymphoma
5 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2014 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 1.000 3 2007 2016
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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.040 1.000 4 2014 2019
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
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
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 1.000 3 2017 2019
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 cancer
CUI: C4048328
Disease: cervical cancer
268 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 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
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 2016
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