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.
Lymphocyte Count measurement
CUI: C0200635
Disease: Lymphocyte Count measurement
456 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.700 1.000 1 2016 2016
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.700 1.000 1 2016 2016
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.700 1.000 1 2019 2019
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.090 0.778 9 2004 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.080 1.000 8 2005 2014
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
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.040 1.000 4 2005 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.030 1.000 3 2006 2011
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.030 1.000 3 2003 2016
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
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.020 1.000 2 2014 2018
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
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.020 1.000 2 2008 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.020 1.000 2 2008 2012
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.020 1.000 2 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
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
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
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
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
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
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
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