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.
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.050 1.000 5 2010 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.050 0.800 5 2010 2020
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
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
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.040 1.000 4 2017 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.040 1.000 4 2013 2018
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.040 0.750 4 2015 2020
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
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
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
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 1.000 3 2012 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 1.000 3 2014 2016
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 0.667 3 2018 2019
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 prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 0.667 3 2011 2017
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 1.000 3 2013 2017
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 0.667 3 2011 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
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
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 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
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2011 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 2016