ANGPTL4, angiopoietin like 4, 51129

N. diseases: 198; N. variants: 8
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7255436
rs7255436 		19 8368312 intron variant C/A snv 0.55
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2010 2018
dbSNP: rs7255436
rs7255436 		19 8368312 intron variant C/A snv 0.55
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2010 2013
dbSNP: rs587777517
rs587777517 		19 8369320 stop gained A/T snv 7.0E-06
CUI: C4014553
Disease: PLASMA TRIGLYCERIDE LEVEL QUANTITATIVE TRAIT LOCUS
PLASMA TRIGLYCERIDE LEVEL QUANTITATIVE TRAIT LOCUS 		0.700 0
dbSNP: rs4076317
rs4076317 		0.882 0.080 19 8364115 intron variant C/G snv 0.25
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4076317
rs4076317 		0.882 0.080 19 8364115 intron variant C/G snv 0.25
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs4076317
rs4076317 		0.882 0.080 19 8364115 intron variant C/G snv 0.25
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4076317
rs4076317 		0.882 0.080 19 8364115 intron variant C/G snv 0.25
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs4076317
rs4076317 		0.882 0.080 19 8364115 intron variant C/G snv 0.25
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2278236
rs2278236 		19 8366697 intron variant G/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2012 2019
dbSNP: rs2278236
rs2278236 		19 8366697 intron variant G/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs117760119
rs117760119 		19 8367853 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2019 2019
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 7 2014 2019
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 7 2014 2019
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.030 0.667 3 2008 2016
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.030 1.000 3 2008 2009
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.030 0.667 3 2008 2016
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.030 1.000 3 2008 2009
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.710 1.000 3 2016 2018
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2016 2018
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.020 1.000 2 2016 2019
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.020 1.000 2 2011 2016
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs116843064
rs116843064 		0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019