rs281432, ICAM1

N. diseases: 12
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.
Angina Pectoris
CUI: C0002962
Disease: Angina Pectoris
65 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2015 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2016 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2015 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2015 2015
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2006 2006
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2006 2006
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2015 2015
invasive cancer
CUI: C0677898
Disease: invasive cancer
15 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1 2016 2016
precancerous lesions
CUI: C0940937
Disease: precancerous lesions
19 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2016 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1 2016 2016
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.851 0.280 19 10279982 intron variant C/G snv 0.52 0.010 1.000 1 2013 2013