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
676 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.800 7 2011 2017
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
814 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.800 6 2012 2017
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
52 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.800 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.710 1.000 3 2013 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.710 1.000 2 2010 2017
Apolipoprotein E, Deficiency or Defect of
7 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 3 1994 2004
Dysbetalipoproteinemia due to Defect in Apolipoprotein E-d
7 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 3 1994 2004
Familial Hyperbeta- and Prebetalipoproteinemia
7 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 3 1994 2004
Floating-Betalipoproteinemia
CUI: C1862562
Disease: Floating-Betalipoproteinemia
7 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 3 1994 2004
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
8 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 3 1994 2004
Hyperlipoproteinemia Type III
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
15 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 3 1994 2004
Hyperlipemia with Familial Hypercholesterolemic Xanthomatosis
7 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 3 1994 2004
Broad-Betalipoproteinemia
CUI: C1862561
Disease: Broad-Betalipoproteinemia
7 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 3 1994 2004
LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5
7 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 3 1994 2004
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2017 2017
Lipoprotein (a) measurement
CUI: C1096202
Disease: Lipoprotein (a) measurement
88 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2017 2017
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
91 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2017 2017
Ischemic cardiomyopathy
CUI: C0349782
Disease: Ischemic cardiomyopathy
65 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2017 2017
High density lipoprotein measurement
867 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2017 2017
Angina Pectoris
CUI: C0002962
Disease: Angina Pectoris
64 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2017 2017
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
735 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2013 2013
response to statin
CUI: C3549252
Disease: response to statin
166 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2012 2012
RDW - Red blood cell distribution width result
206 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2017 2017
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
472 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2017 2017
Red cell distribution width determination
206 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.700 1 2017 2017