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rs2000813

From SNPedia

Orientationplus
Stabilizedplus
Make rs2000813(C;C)
Make rs2000813(C;T)
Make rs2000813(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position49567494
GeneLIPG
is asnp
is mentioned by
dbSNPrs2000813
dbSNP (classic)rs2000813
ClinGenrs2000813
ebirs2000813
HLIrs2000813
Exacrs2000813
Gnomadrs2000813
Varsomers2000813
LitVarrs2000813
Maprs2000813
PheGenIrs2000813
Biobankrs2000813
1000 genomesrs2000813
hgdprs2000813
ensemblrs2000813
geneviewrs2000813
scholarrs2000813
googlers2000813
pharmgkbrs2000813
gwascentralrs2000813
openSNPrs2000813
23andMers2000813
SNPshotrs2000813
SNPdbers2000813
MSV3drs2000813
GWAS Ctlgrs2000813
GMAF0.2438
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19380136OA-icon.png] Physical inactivity interacts with an endothelial lipase polymorphism to modulate high density lipoprotein cholesterol in the GOLDN study


[PMID 20466371] Lack of association between common genetic variation in endothelial lipase (LIPG) and the risk for CAD and DVT

[PMID 20923576OA-icon.png] Association of the LIPG 584C>T polymorphism and serum lipid levels in the Guangxi Bai Ku Yao and Han populations


[PMID 22174694OA-icon.png] Mining the LIPG Allelic Spectrum Reveals the Contribution of Rare and Common Regulatory Variants to HDL Cholesterol


[PMID 18078817OA-icon.png] Multiple genetic determinants of plasma lipid levels in Caribbean Hispanics.


[PMID 19041386OA-icon.png] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.


[PMID 19287092OA-icon.png] Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans.


[PMID 21145773] Association of endothelial lipase Thr111Ile polymorphism with lipid metabolism and microvascular complications in type 2 diabetic patients.


[PMID 21816559] Interactions of the LIPG 584C>T polymorphism and alcohol consumption on serum lipid levels.



[PMID 23355348] Interactions of several single nucleotide polymorphisms and high body mass index on serum lipid traits.


[PMID 24852509] Association of endothelial lipase Thr111Ile polymorphism with proliferative retinopathy in type 2 diabetes patients


[PMID 26124511OA-icon.png] Association of endothelial lipase gene-384A/C with coronary artery disease in Han Chinese people