rs1799864, CCR2

N. diseases: 68
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.
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.700 1.000 1 2016 2016
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.700 1.000 1 2016 2016
Acquired Immunodeficiency Syndrome
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
42 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2002 2002
Adrenoleukodystrophy
CUI: C0162309
Disease: Adrenoleukodystrophy
116 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2012 2012
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2004 2004
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2018 2018
Anthracosis
CUI: C0003165
Disease: Anthracosis
37 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2006 2006
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2011 2011
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2006 2006
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2006 2006
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2016 2016
Carotid Artery Plaque
CUI: C0751633
Disease: Carotid Artery Plaque
3 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2009 2009
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2009 2009
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2012 2012
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2016 2016
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2012 2012
Common Migraine
CUI: C0338480
Disease: Common Migraine
62 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2009 2009
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2013 2013
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2002 2002
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2010 2010
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2004 2004
HER2-negative breast cancer
CUI: C4733095
Disease: HER2-negative breast cancer
18 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2016 2016
HER2-positive carcinoma of breast
CUI: C1960398
Disease: HER2-positive carcinoma of breast
26 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2016 2016
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2010 2010
Infiltrating Cervical Carcinoma
CUI: C1334177
Disease: Infiltrating Cervical Carcinoma
13 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2010 2010