rs1800872, IL19;IL10

N. diseases: 119
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.
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
527 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.700 0
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2012 2012
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1 2013 2013
Acute pyelonephritis
CUI: C0520575
Disease: Acute pyelonephritis
10 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2014 2014
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2015 2015
African Burkitt's lymphoma
CUI: C0343640
Disease: African Burkitt's lymphoma
5 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2014 2014
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2015 2015
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2010 2010
Asthma
CUI: C0004096
Disease: Asthma
1536 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2016 2016
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2010 2010
Autoimmune Chronic Hepatitis
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
23 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2018 2018
Autoimmune hepatitis
CUI: C4721555
Disease: Autoimmune hepatitis
22 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2018 2018
Autoimmune liver disease
CUI: C0400936
Disease: Autoimmune liver disease
3 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1 2018 2018
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2016 2016
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2018 2018
Boutonneuse Fever
CUI: C0006060
Disease: Boutonneuse Fever
3 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2009 2009
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2018 2018
Brucellosis
CUI: C0006309
Disease: Brucellosis
30 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1 2020 2020
Calcific stenosis
CUI: C0333184
Disease: Calcific stenosis
4 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2014 2014
Cancer of Nasopharynx
CUI: C0238301
Disease: Cancer of Nasopharynx
12 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2016 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2014 2014
CATARACT, ANTERIOR POLAR
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
27 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2016 2016
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2017 2017
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2016 2016
Chronic gastritis
CUI: C0085695
Disease: Chronic gastritis
11 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2015 2015