rs662799, APOA5

N. diseases: 33
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.
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2019 2019
Anemia
CUI: C0002871
Disease: Anemia
94 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2018 2018
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2020 2020
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2018 2018
Atherogenic dyslipidaemia
CUI: C4524040
Disease: Atherogenic dyslipidaemia
9 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2015 2015
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2018 2018
Avascular Necrosis of Femur Head
CUI: C0410480
Disease: Avascular Necrosis of Femur Head
20 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2014 2014
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2018 2018
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2014 2014
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.030 1.000 3 2010 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.070 1.000 7 2010 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.030 1.000 3 2010 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2014 2014
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.020 1.000 2 2012 2014
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.020 1.000 2 2011 2014
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.030 1.000 3 2012 2016
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2017 2017
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.800 1.000 7 2012 2019
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.030 1.000 3 2014 2018
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2018 2018
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.060 1.000 6 2012 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.100 0.900 10 2011 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2011 2011
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1 2018 2018