LIPG, lipase G, endothelial type, 9388

N. diseases: 62; N. variants: 18
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35816125
rs35816125
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASCAT Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis. 30805717 2019
dbSNP: rs35816125
rs35816125
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0002395
Disease:
Alzheimer's Disease 		0.700 GeneticVariation GWASCAT Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis. 30805717 2019
dbSNP: rs77960347
rs77960347
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs77960347
rs77960347
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11082764
rs11082764
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs12970066
rs12970066
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		C 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs149615216
rs149615216
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C1445957
Disease:
Serum total cholesterol measurement 		C 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs149615216
rs149615216
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		C 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs3786247
rs3786247
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C1445957
Disease:
Serum total cholesterol measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs77960347
rs77960347
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C1445957
Disease:
Serum total cholesterol measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs77960347
rs77960347
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs77960347
rs77960347
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs77960347
rs77960347
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C1445957
Disease:
Serum total cholesterol measurement 		A 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs77960347
rs77960347
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs149615216
rs149615216
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.700 GeneticVariation GWASCAT Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. 28270201 2017
dbSNP: rs201922257
rs201922257
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0202177
Disease:
Phospholipid measurement 		0.700 GeneticVariation GWASCAT Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. 29084231 2017
dbSNP: rs201922257
rs201922257
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASCAT Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. 29084231 2017
dbSNP: rs3786247
rs3786247
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.700 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs9958734
rs9958734
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C1445957
Disease:
Serum total cholesterol measurement 		T 0.700 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs12970066
rs12970066
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		G 0.700 GeneticVariation GWASCAT Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations. 26582766 2016
dbSNP: rs149615216
rs149615216
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C1445957
Disease:
Serum total cholesterol measurement 		T 0.700 GeneticVariation GWASCAT The impact of low-frequency and rare variants on lipid levels. 25961943 2015
dbSNP: rs77960347
rs77960347
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASCAT Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. 24507774 2014
dbSNP: rs11875600
rs11875600
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs11875600
rs11875600
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs12966382
rs12966382
Entrez Id: 9388
Gene Symbol: LIPG
LIPG
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012