rs1800871, IL19;IL10

N. diseases: 108
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.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.830 0.800 5 2010 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.040 0.750 4 2012 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.040 0.750 4 2012 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.040 1.000 4 2011 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.040 1.000 4 2011 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2007 2016
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2015 2016
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2015 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2015 2018
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2009 2016
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2010 2014
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2014 2018
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2015 2017
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 0.500 2 2015 2016
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 0.500 2 2015 2016
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2015 2019
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 0.500 2 2013 2019
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2015 2018
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2008 2016
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2010 2015
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 0.500 2 2015 2016
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2008 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2010 2013
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2015 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 0.500 2 2017 2019