Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		G 0.800 GeneticVariation GWASCAT Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs964184
rs964184
ZPR1
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		G 0.800 GeneticVariation GWASCAT Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009
dbSNP: rs964184
rs964184
ZPR1
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		G 0.830 GeneticVariation GWASCAT 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 GWASCAT 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 GWASCAT 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 GWASCAT 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 GWASCAT Genetic variants influencing circulating lipid levels and risk of coronary artery disease. 20864672

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

2010
dbSNP: rs964184
rs964184
ZPR1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		G 0.830 GeneticVariation GWASCAT Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990

2011
dbSNP: rs964184
rs964184
ZPR1
CUI: C1142098
Disease: Vitamin E Assay
Vitamin E Assay 		G 0.800 GeneticVariation GWASCAT In genome-wide association studies (GWAS) of common genetic variants associated with circulating alpha- and gamma-tocopherol concentrations in two adult cohorts comprising 5006 men of European descent, we observed three loci associated with alpha-tocopherol levels, two novel single-nucleotide polymorphisms (SNPs), rs2108622 on 19pter-p13.11 (P= 1.7 × 10(-8)) and rs11057830 on 12q24.31 (P= 2.0 × 10(-8)) and confirmed a previously reported locus marked by rs964184 on 11q23.3 (P= 2.7 × 10(-10)). 21729881

2011
dbSNP: rs964184
rs964184
ZPR1
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		G 0.810 GeneticVariation GWASCAT A previously known lipid locus, APOA1/C3/A4/A5 gene cluster region (SNP rs964184), was associated with MetS in all 4 study samples (P=7.23×10(-9) in meta-analysis). 22399527

2012
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.800 GeneticVariation GWASCAT Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. 22359512

2012
dbSNP: rs964184
rs964184
ZPR1
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 GeneticVariation GWASCAT Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis. 22916037

2012
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 GeneticVariation GWASCAT Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci. 23505323

2013
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		C 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068

2013
dbSNP: rs964184
rs964184
ZPR1
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		C 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068

2013
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 GeneticVariation GWASCAT Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. 23696881

2013
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		C 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068

2013
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		G 0.800 GeneticVariation GWASCAT Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. 23726366

2013
dbSNP: rs964184
rs964184
ZPR1
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		G 0.800 GeneticVariation GWASCAT Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. 23726366

2013
dbSNP: rs964184
rs964184
ZPR1
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		C 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068

2013
dbSNP: rs964184
rs964184
ZPR1
CUI: C0428580
Disease: Vitamin measurement
Vitamin measurement 		0.700 GeneticVariation GWASCAT Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. 23696881

2013
dbSNP: rs964184
rs964184
ZPR1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.830 GeneticVariation GWASCAT Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325

2014
dbSNP: rs964184
rs964184
ZPR1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		G 0.800 GeneticVariation GWASCAT Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. 24886709

2014
dbSNP: rs964184
rs964184
ZPR1
CUI: C0042879
Disease: Vitamin K Assay
Vitamin K Assay 		G 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for circulating phylloquinone concentrations. 25411281

2014