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.
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 2016
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2012 2019
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 2016
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 2019
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2019 2019
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 2019
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2014 2016
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 2016
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2008 2010
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2009 2014
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 2016
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2014 2016
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2011 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2015 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 0.500 2 2017 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 2 2017 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2007 2011
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2010 2016
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2010 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2011 2018
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2016 2017
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