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.
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
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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 0.500 2 2003 2003
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2003 2003
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2004 2004
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 0.500 2 2003 2005
Biliary Atresia
CUI: C0005411
Disease: Biliary Atresia
32 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
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
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2006 2006
Primary sclerosing cholangitis
CUI: C0566602
Disease: Primary sclerosing cholangitis
58 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2004 2006
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
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2006 2006
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2006 2006
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
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
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 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
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
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2008 2008
Proliferative diabetic retinopathy
CUI: C0154830
Disease: Proliferative diabetic retinopathy
45 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2008 2008
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2009 2009
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
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2009 2009
Malignant neoplasm of colon and/or rectum
502 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2009 2009