rs17321515, None

N. diseases: 16
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.800 1.000 4 2008 2019
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.800 1.000 3 2012 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.800 1.000 3 2012 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.730 0.750 4 2009 2019
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.700 1.000 1 2012 2012
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.700 1.000 1 2012 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.020 1.000 2 2009 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.020 1.000 2 2009 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.020 1.000 2 2011 2019
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.020 1.000 2 2019 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.010 1.000 1 2009 2009
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.010 1.000 1 2011 2011
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.010 1.000 1 2009 2009
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.010 1.000 1 2011 2011
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.010 1.000 1 2011 2011