Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6589566
rs6589566
ZPR1
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. 18179892

2008
dbSNP: rs6589566
rs6589566
ZPR1
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		G 0.700 GeneticVariation GWASDB Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. 18179892

2008
dbSNP: rs12286037
rs12286037
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		T 0.800 GeneticVariation GWASDB Newly identified loci that influence lipid concentrations and risk of coronary artery disease. 18193043

2008
dbSNP: rs964184
rs964184
ZPR1
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		G 0.800 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		G 0.800 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs964184
rs964184
ZPR1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		G 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs35120633
rs35120633
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 GeneticVariation GWASDB Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911

2009
dbSNP: rs964184
rs964184
ZPR1
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		G 0.830 GeneticVariation GWASDB Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. 20657596

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		G 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		G 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		G 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		G 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		G 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		G 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		G 0.800 GeneticVariation GWASDB Genetic variants influencing circulating lipid levels and risk of coronary artery disease. 20864672

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		G 0.700 GeneticVariation GWASDB Genetic variants influencing circulating lipid levels and risk of coronary artery disease. 20864672

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.830 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282

2011
dbSNP: rs6589566
rs6589566
ZPR1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282

2011
dbSNP: rs964184
rs964184
ZPR1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		G 0.830 GeneticVariation GWASDB Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990

2011
dbSNP: rs2266788
rs2266788
ZPR1 ; APOA5
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011
dbSNP: rs2266788
rs2266788
ZPR1 ; APOA5
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		A 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011
dbSNP: rs2266788
rs2266788
ZPR1 ; APOA5
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011
dbSNP: rs2075290
rs2075290
ZPR1
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011
dbSNP: rs2075290
rs2075290
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011
dbSNP: rs12286037
rs12286037
ZPR1
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011