rs3732379, CX3CR1

N. diseases: 38
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.
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.080 0.875 8 2004 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.080 1.000 8 2001 2014
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.030 1.000 3 2006 2016
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.030 1.000 3 2006 2016
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.030 1.000 3 2003 2016
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.020 1.000 2 2014 2018
Asthma
CUI: C0004096
Disease: Asthma
1536 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.020 1.000 2 2006 2011
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.020 1.000 2 2003 2011
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.020 1.000 2 2008 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.020 1.000 2 2008 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.020 0.500 2 2009 2016
Acquired Immunodeficiency Syndrome
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
42 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2005 2005
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2005 2005
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2005 2005
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2012 2012
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2018 2018
Anthracosis
CUI: C0003165
Disease: Anthracosis
37 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2006 2006
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1 2005 2005
Cardiovascular Abnormalities
CUI: C0243050
Disease: Cardiovascular Abnormalities
12 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2003 2003
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1 2009 2009
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2005 2005
Chronic tonsillitis
CUI: C0149517
Disease: Chronic tonsillitis
3 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2014 2014
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2008 2008
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2016 2016
Geographic Atrophy
CUI: C1536085
Disease: Geographic Atrophy
81 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2012 2012