CX3CR1, C-X3-C motif chemokine receptor 1, 1524

N. diseases: 310; N. variants: 10
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0003165
Disease: Anthracosis
Anthracosis 		Respiratory Tract Diseases 0.010 1.000 1 2006 2006
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C2827407
Disease: Infectious Otitis Media
Infectious Otitis Media 		Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0243050
Disease: Cardiovascular Abnormalities
Cardiovascular Abnormalities 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2003 2003
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0271429
Disease: Acute otitis media
Acute otitis media 		Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0276340
Disease: Respiratory syncytial virus bronchiolitis
Respiratory syncytial virus bronchiolitis 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2006 2006
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2009 2009
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2005 2005
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2006 2006
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		Cardiovascular Diseases 0.010 < 0.001 1 2003 2003
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0041912
Disease: Upper Respiratory Infections
Upper Respiratory Infections 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0030481
Disease: Tropical Spastic Paraparesis
Tropical Spastic Paraparesis 		Infections; Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs3732378
rs3732378 		0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2012 2012