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.
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
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
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
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
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
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
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
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
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
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
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
Tropical Spastic Paraparesis
CUI: C0030481
Disease: Tropical Spastic Paraparesis
4 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2008 2008
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
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
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
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
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
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
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