|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
22843504 |
2012 |
|
Coronary Artery Disease
|
|
0.030 |
GeneticVariation
|
BEFREE |
To investigate the relationship between the common single nucleotide polymorphisms (SNPs) 584C/T (rs2000813) and -384A/C (rs3813082) in the LIPG gene and CAD, allele and genotype frequencies of the two SNPs were analysed in 287 Chinese patients with CAD and 367 controls by the high-resolution melting curve (HRM) method.
|
26124511 |
2015 |
|
Coronary Artery Disease
|
|
0.030 |
GeneticVariation
|
BEFREE |
Our data support a modest association between the LIPG rs2000813 variant and parameters of HDL metabolism, but no association between common genetic variants in LIPG and CAD or DVT risk.
|
20466371 |
2010 |
|
Coronary Artery Disease
|
|
0.030 |
GeneticVariation
|
BEFREE |
The T111I variant in the endothelial lipase gene and risk of coronary heart disease in three independent populations.
|
19411665 |
2009 |
|
Diabetes Mellitus, Non-Insulin-Dependent
|
|
0.020 |
GeneticVariation
|
BEFREE |
In hyperlipidemic patients, apart from its known association with HDL-C, CETP Taq1B is also associated with A1C levels, and both associations are modified by type 2 diabetes and LIPG Thr111Ile.
|
27590083 |
2016 |
|
Diabetes Mellitus, Non-Insulin-Dependent
|
|
0.020 |
GeneticVariation
|
BEFREE |
Association of endothelial lipase Thr111Ile polymorphism with proliferative retinopathy in type 2 diabetes patients.
|
24852509 |
2014 |
|
Diabetic Retinopathy
|
|
0.010 |
GeneticVariation
|
BEFREE |
Our previous study demonstrated that the endothelial lipase (EL) C.584C>T polymorphism (rs2000813, p.Thr111Ile) was significantly associated with diabetic retinopathy (DR).
|
24852509 |
2014 |
|
Proliferative retinopathy
|
|
0.010 |
GeneticVariation
|
BEFREE |
Association of endothelial lipase Thr111Ile polymorphism with proliferative retinopathy in type 2 diabetes patients.
|
24852509 |
2014 |
|
Deep Vein Thrombosis
|
|
0.010 |
GeneticVariation
|
BEFREE |
Our data support a modest association between the LIPG rs2000813 variant and parameters of HDL metabolism, but no association between common genetic variants in LIPG and CAD or DVT risk.
|
20466371 |
2010 |
|
Coronary heart disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
Our analysis among healthy Caucasian men and women from three independent studies does not support an association between the T111I variant and HDL-C, other plasma lipids, or risk of CHD.
|
19411665 |
2009 |
|
Metabolic Syndrome X
|
|
0.010 |
GeneticVariation
|
BEFREE |
We examined associations between variants LIPG T111I (rs2000813) and LIPG i24582 (rs6507931), HDL and television viewing/computer use ("screen time") as a marker for physical inactivity in a population with high prevalence of metabolic syndrome.
|
19380136 |
2009 |
|
Coronary Arteriosclerosis
|
|
0.010 |
GeneticVariation
|
BEFREE |
The T111I variant in the endothelial lipase gene and risk of coronary heart disease in three independent populations.
|
19411665 |
2009 |