rs5498, ICAM4;ICAM1

N. diseases: 99
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.
Brain Abscess
CUI: C0006105
Disease: Brain Abscess
1 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Cerebral abscess
CUI: C1510428
Disease: Cerebral abscess
1 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Decompensated cirrhosis of liver
CUI: C1619727
Disease: Decompensated cirrhosis of liver
2 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2008 2008
Peripheral arterial occlusive disease
3 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2002 2002
Retinoic acid syndrome
CUI: C0860564
Disease: Retinoic acid syndrome
3 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2007 2007
Aneurysm, Dissecting
CUI: C0002949
Disease: Aneurysm, Dissecting
4 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2006 2006
Chronic thromboembolic pulmonary hypertension
4 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2019 2019
Japanese Encephalitis
CUI: C0014057
Disease: Japanese Encephalitis
6 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2018 2018
neurological disability
CUI: C0848771
Disease: neurological disability
6 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2017 2017
Polymyalgia Rheumatica
CUI: C0032533
Disease: Polymyalgia Rheumatica
7 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2000 2000
Diffuse Astrocytoma
CUI: C0280785
Disease: Diffuse Astrocytoma
8 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2009 2009
Neurocysticercosis
CUI: C0338437
Disease: Neurocysticercosis
9 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2014 2014
Obstructive azoospermia
CUI: C4023106
Disease: Obstructive azoospermia
9 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2019 2019
Acute pyelonephritis
CUI: C0520575
Disease: Acute pyelonephritis
10 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2018 2018
Urinary tract infection
CUI: C0042029
Disease: Urinary tract infection
14 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2018 2018
invasive cancer
CUI: C0677898
Disease: invasive cancer
15 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Malignant neoplasm of brain
CUI: C0153633
Disease: Malignant neoplasm of brain
16 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2013 2013
Chronic graft-versus-host disease
CUI: C0867389
Disease: Chronic graft-versus-host disease
17 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2013 2013
Icterus
CUI: C0022346
Disease: Icterus
17 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2005 2005
Congenital atresia of extrahepatic bile duct
19 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2005 2005
precancerous lesions
CUI: C0940937
Disease: precancerous lesions
19 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Acute Promyelocytic Leukemia
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
21 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2007 2007
Angina, Unstable
CUI: C0002965
Disease: Angina, Unstable
21 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2008 2008
Vasculitis
CUI: C0042384
Disease: Vasculitis
24 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Acromegaly
CUI: C0001206
Disease: Acromegaly
25 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2015 2015