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.
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
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: 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
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2018 2018
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
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
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2010 2010
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
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
Common Migraine
CUI: C0338480
Disease: Common Migraine
62 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2014 2014
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 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 liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Non-obstructive azoospermia
CUI: C4021107
Disease: Non-obstructive azoospermia
88 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2019 2019
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
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
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
129 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2014 2014
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2012 2012
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2016 2016
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2012 2012
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2013 2013
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.060 0.500 6 2006 2018
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2019 2019
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.050 1.000 5 2006 2018