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.
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2011 2011
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
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
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
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
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2016 2016
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
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2013 2013
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
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2012 2012
Obesity
CUI: C0028754
Disease: Obesity
1111 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2014 2014
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 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
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2013 2013
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
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
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
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2015 2015
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
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