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.
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
Hepatocarcinogenesis
CUI: C1512409
Disease: Hepatocarcinogenesis
24 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2005 2005
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1 2009 2009
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1 2005 2005
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2012 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2016 2016
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1 2005 2005
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1 2005 2005
Obesity
CUI: C0028754
Disease: Obesity
1111 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2014 2014
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2012 2012
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2003 2003
Stenosis of intestine
CUI: C0267465
Disease: Stenosis of intestine
3 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2008 2008