rs3732378, CX3CR1

N. diseases: 48
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.
Acute otitis media
CUI: C0271429
Disease: Acute otitis media
1 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2014 2014
Respiratory syncytial virus bronchiolitis
CUI: C0276340
Disease: Respiratory syncytial virus bronchiolitis
1 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2006 2006
Chronic tonsillitis
CUI: C0149517
Disease: Chronic tonsillitis
3 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2014 2014
Stenosis of intestine
CUI: C0267465
Disease: Stenosis of intestine
3 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2006 2006
Tropical Spastic Paraparesis
CUI: C0030481
Disease: Tropical Spastic Paraparesis
4 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2008 2008
Infectious Otitis Media
CUI: C2827407
Disease: Infectious Otitis Media
6 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2014 2014
Upper Respiratory Infections
CUI: C0041912
Disease: Upper Respiratory Infections
6 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2014 2014
Cardiovascular Abnormalities
CUI: C0243050
Disease: Cardiovascular Abnormalities
12 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2003 2003
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
CUI: C0375023
Disease: Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
14 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2006 2006
Endothelial dysfunction
CUI: C0856169
Disease: Endothelial dysfunction
25 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2009 2009
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2006 2006
Anthracosis
CUI: C0003165
Disease: Anthracosis
37 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2006 2006
Acquired Immunodeficiency Syndrome
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
42 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2005 2005
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2005 2005
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1 2009 2009
Geographic Atrophy
CUI: C1536085
Disease: Geographic Atrophy
81 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2012 2012
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2012 2012
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1 2003 2003
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.020 1.000 2 2005 2018
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.020 1.000 2 2005 2018
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2008 2008
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.020 1.000 2 2003 2011
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2018 2018
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.040 1.000 4 2005 2016
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
269 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2011 2011