rs579459, None

N. diseases: 28
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.
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.800 1.000 6 2013 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.800 1.000 5 2013 2019
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.800 1.000 3 2011 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.800 1.000 2 2011 2014
Alkaline phosphatase measurement
CUI: C0201850
Disease: Alkaline phosphatase measurement
79 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.800 1.000 1 2011 2011
E-selectin Measurement
CUI: C4722217
Disease: E-selectin Measurement
6 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.800 1.000 1 2009 2009
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 2 2012 2017
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2018 2018
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2012 2012
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2014 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2014 2014
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2013 2013
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2012 2012
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2013 2013
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2012 2012
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2013 2013
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2013 2013
Soluble P-Selectin Measurement
CUI: C4050627
Disease: Soluble P-Selectin Measurement
3 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2010 2010
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2012 2012
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.700 1.000 1 2013 2013
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.010 1.000 1 2013 2013
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.010 1.000 1 2018 2018
Large-artery atherosclerosis (embolus/thrombosis)
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
35 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.010 1.000 1 2016 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.010 1 2014 2014