rs201058276, F7

N. diseases: 11
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.050 1.000 5 2000 2013
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.030 1.000 3 2000 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.030 1.000 3 2000 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.030 0.667 3 2001 2007
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.020 1.000 2 2001 2002
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.020 1.000 2 2001 2004
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.010 1 2002 2002
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.010 1.000 1 2004 2004
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.010 1.000 1 2004 2004
Thrombosis of cerebral veins
CUI: C0151945
Disease: Thrombosis of cerebral veins
11 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.010 1.000 1 2012 2012
Vertical Talus
CUI: C0240912
Disease: Vertical Talus
20 0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 0.010 1 2012 2012