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: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 8 2012 2019
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 7 2012 2019
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 3 2012 2019
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.100 0.900 10 2011 2017
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.070 1.000 7 2010 2019
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.060 1.000 6 2012 2018
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0028754
Disease: Obesity
Obesity 		0.050 1.000 5 2011 2015
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 1.000 3 2014 2018
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.030 1.000 3 2010 2016
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.030 1.000 3 2012 2016
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.030 1.000 3 2010 2016
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.020 1.000 2 2012 2014
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 1.000 2 2011 2014
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0410480
Disease: Avascular Necrosis of Femur Head
Avascular Necrosis of Femur Head 		0.010 1.000 1 2014 2014
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.010 < 0.001 1 2018 2018
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0002871
Disease: Anemia
Anemia 		0.010 1.000 1 2018 2018
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.010 1.000 1 2020 2020
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2018 2018
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2014 2014
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2011 2011
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		0.010 1.000 1 2018 2018