Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1260326
rs1260326
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
T 0.800 GeneticVariation GWASCAT Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. 21943158

2011

dbSNP: rs1260326
rs1260326
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
T 0.800 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. 21300955

2011

dbSNP: rs1260326
rs1260326
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
T 0.800 GeneticVariation GWASCAT New gene functions in megakaryopoiesis and platelet formation. 22139419

2011

dbSNP: rs1260326
rs1260326
Serum gamma-glutamyl transferase measurement
T 0.800 GeneticVariation GWASCAT Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. 22001757

2011

dbSNP: rs780093
rs780093
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
A 0.700 GeneticVariation GWASCAT A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

dbSNP: rs780093
rs780093
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
A 0.700 GeneticVariation GWASCAT A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

dbSNP: rs780094
rs780094
Diabetes Mellitus, Non-Insulin-Dependent
C 0.900 GeneticVariation GWASCAT Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922

2012

dbSNP: rs780094
rs780094
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
A 0.830 GeneticVariation GWASCAT Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. 22399527

2012

dbSNP: rs780094
rs780094
CUI: C1305855
Disease: Body mass index
Body mass index
T 0.800 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228

2012

dbSNP: rs780094
rs780094
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
T 0.800 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228

2012

dbSNP: rs1260326
rs1260326
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
C 0.800 GeneticVariation GWASCAT Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069

2012

dbSNP: rs1260326
rs1260326
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
T 0.800 GeneticVariation GWASCAT Discovery and fine mapping of serum protein loci through transethnic meta-analysis. 23022100

2012

dbSNP: rs780094
rs780094
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
T 0.700 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228

2012

dbSNP: rs780094
rs780094
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
T 0.700 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228

2012

dbSNP: rs780093
rs780093
Sex hormone binding globulin measurement
T 0.700 GeneticVariation GWASCAT Loci near the identified SNPs included SHBG (rs12150660, 17p13.1, p = 1.8 × 10(-106)), PRMT6 (rs17496332, 1p13.3, p = 1.4 × 10(-11)), GCKR (rs780093, 2p23.3, p = 2.2 × 10(-16)), ZBTB10 (rs440837, 8q21.13, p = 3.4 × 10(-09)), JMJD1C (rs7910927, 10q21.3, p = 6.1 × 10(-35)), SLCO1B1 (rs4149056, 12p12.1, p = 1.9 × 10(-08)), NR2F2 (rs8023580, 15q26.2, p = 8.3 × 10(-12)), ZNF652 (rs2411984, 17q21.32, p = 3.5 × 10(-14)), TDGF3 (rs1573036, Xq22.3, p = 4.1 × 10(-14)), LHCGR (rs10454142, 2p16.3, p = 1.3 × 10(-07)), BAIAP2L1 (rs3779195, 7q21.3, p = 2.7 × 10(-08)), and UGT2B15 (rs293428, 4q13.2, p = 5.5 × 10(-06)). 22829776

2012

dbSNP: rs1260326
rs1260326
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: rs780094
rs780094
CUI: C0201925
Disease: Calcium measurement
Calcium measurement
T 0.800 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. 24068962

2013

dbSNP: rs780094
rs780094
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
C 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: rs780092
rs780092
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
A 0.800 GeneticVariation GWASCAT Genetic association with lipids in Filipinos: waist circumference modifies an APOA5 effect on triglyceride levels. 24023260

2013

dbSNP: rs1260326
rs1260326
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
T 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068

2013

dbSNP: rs1260326
rs1260326
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
T 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068

2013

dbSNP: rs1260326
rs1260326
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
T 0.800 GeneticVariation GWASCAT Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486

2013

dbSNP: rs1260326
rs1260326
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: rs1260326
rs1260326
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
T 0.800 GeneticVariation GWASCAT Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies. 23903356

2013

dbSNP: rs1260326
rs1260326
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
T 0.800 GeneticVariation GWASCAT A genome wide association study identifies common variants associated with lipid levels in the Chinese population. 24386095

2013