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.
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
Nuchal bleb, familial
CUI: C0948242
Disease: Nuchal bleb, familial
9 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2010 2010
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
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
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
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
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
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
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
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.700 1.000 1 2012 2012
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
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
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
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.700 1.000 1 2018 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
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
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.700 1.000 2 2012 2012
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
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
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
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
Obesity
CUI: C0028754
Disease: Obesity
1111 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.050 1.000 5 2011 2015