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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.030 0.667 3 2009 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.030 0.667 3 2009 2017
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.020 1.000 2 2012 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.020 1.000 2 2011 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.020 1.000 2 2015 2015
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.010 1.000 1 2015 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.010 1.000 1 2017 2017
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.010 1.000 1 2013 2013
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.010 1.000 1 2013 2013
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.010 1.000 1 2013 2013
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.776 0.320 3 159988493 intron variant T/G snv 0.10 0.010 1.000 1 2010 2010