Source: ALL

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: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.020 0.500 2 2007 2012
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2006 2006
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2014 2014
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2006 2006
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2014 2014
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2003 2003
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2015 2015
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		0.010 < 0.001 1 2008 2008
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		0.010 1.000 1 2018 2018
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia 		0.010 1.000 1 2008 2008
dbSNP: rs2066714
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2008 2008