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.
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
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.050 1.000 5 2003 2019
Asthma
CUI: C0004096
Disease: Asthma
1536 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.030 1.000 3 2006 2014
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.030 1.000 3 2013 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.030 1.000 3 2006 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.030 1.000 3 2014 2019
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2005 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2005 2012
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2010 2016
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2014 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2004 2012
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
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2019 2019
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2011 2016
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 1.000 2 2004 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
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
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
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
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
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
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
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.700 1.000 1 2018 2018
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