Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.800 1.000 2 2011 2019
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2014
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2013 2019
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C4722217
Disease: E-selectin Measurement
E-selectin Measurement
0.800 1.000 1 2009 2009
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement
0.800 1.000 1 2011 2011
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2013 2019
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2013 2013
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2014 2014
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
0.700 1.000 1 2013 2013
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
0.700 1.000 1 2012 2012
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2013 2013