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.
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
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 2 2007 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 0.500 2 2013 2015
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
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
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 0.500 2 2001 2015
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
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
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
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
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2013 2013
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
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2015 2015
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2014 2014