|
rs964184
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Sixteen SNPs were significantly associated with an increased risk of HTG development, with odds ratios (ORs) (95% confidence interval [CI]) varying from 1.40 (1.01-1.95) to 4.69 (3.29-6.68) (rs964184 within the APOA5 gene).
|
31222479 |
2019 |
|
rs964184
|
|
G |
0.830 |
GeneticVariation |
GWASCAT |
A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.
|
27599772 |
2017 |
|
rs964184
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Multivariate logistic regression analysis with adjustment for age, gender and body mass index revealed that rs964184 of ZPR1 (P=5.1x10‑7; odds ratio, 1.37; dominant model), rs4845625 of IL6R (P=0.0019, odds ratio, 1.25; dominant model) and rs46522 of UBE2Z (P=0.0039, odds ratio, 1.19; dominant model) were significantly associated with hypertriglyceridemia, and that rs599839 of PSRC1 (P=0.0004, odds ratio, 0.70; dominant model) and rs2075650 of TOMM40 (P=0.0004, odds ratio, 1.43; dominant model) were significantly associated with hyper‑LDL‑cholesterolemia.
|
26238946 |
2015 |
|
rs964184
|
|
|
0.830 |
GeneticVariation |
BEFREE |
The G-G-A-A-C-C haplotype, carrying rs964184-G-allele, was associated with increased risk of HCH (OR: 1.35, 95% CI: 1.10, 1.66, P = 0.005) and HTG (OR: 1.75, 95% CI: 1.39, 2.21, P = 0.000).
|
24780069 |
2014 |
|
rs964184
|
|
|
0.830 |
GeneticVariation |
GWASDB |
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
|
23505323 |
2013 |
|
rs964184
|
|
G |
0.830 |
GeneticVariation |
GWASDB |
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
|
20657596 |
2010 |
|
rs964184
|
|
G |
0.830 |
GeneticVariation |
GWASCAT |
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
|
20657596 |
2010 |
|
rs1260326
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Once demographics, medication use and baseline adiposity, and fitness were accounted for, ILI did not modify the baseline association of GCKR-Leu446Pro with elevated triglycerides (β±SE=0.067±0.013, P=1.5×10(-7) and β±SE=0.052±0.015, P=5×10(-4)) or with elevated CRP (β±SE=0.136±0.034, P=5.1×10(-5)and β±SE=0.903±0.038, P=0.015) in the overall sample and Non-Hispanic Whites, respectively.
|
26578543 |
2016 |
|
rs1260326
|
|
|
0.820 |
GeneticVariation |
GWASDB |
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
|
23505323 |
2013 |
|
rs1260326
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Recently, the single nucleotide polymorphism (SNP) identified as rs1260326, in the glucokinase regulatory protein (GCKR), was associated with hypertriglyceridemia in adults.
|
22105854 |
2012 |
|
rs1260326
|
|
T |
0.820 |
GeneticVariation |
GWASDB |
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
|
20657596 |
2010 |
|
rs1260326
|
|
T |
0.820 |
GeneticVariation |
GWASCAT |
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
|
20657596 |
2010 |
|
rs4635554
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
|
20657596 |
2010 |
|
rs4635554
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
|
20657596 |
2010 |
|
rs7016880
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
|
20657596 |
2010 |
|
rs7016880
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
|
20657596 |
2010 |
|
rs780094
|
|
T |
0.730 |
GeneticVariation |
GWASCAT |
A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.
|
27599772 |
2017 |
|
rs780094
|
|
|
0.730 |
GeneticVariation |
BEFREE |
The T2D risk alleles of rs972283 near KLF14 and rs11634397 near ZFAND6 were associated with a higher risk for elevated triglycerides (rs972283: 1.11 (1.02, 1.24), P = 1.46 × 10-2; rs11634397: 1.14 (1.00, 1.29), P = 4.66 × 10-2), while the T2D risk alleles of rs780094 in GCKR and rs7903146 in TCF7L2 were related to a lower risk of elevated triglycerides (rs780094: 0.86 (0.80, 0.93), P = 1.35 × 10-4; rs7903146: 0.82 (0.69, 0.98), P = 3.18 × 10-2).
|
26599349 |
2015 |
|
rs780094
|
|
|
0.730 |
GeneticVariation |
BEFREE |
GCKR rs780094 was also associated with decreased plasma glucose, and increased triglycerides in the patient and control groups.
|
24785259 |
2014 |
|
rs780094
|
|
|
0.730 |
GeneticVariation |
BEFREE |
The GCKR rs780094 polymorphism is associated with susceptibility of type 2 diabetes, reduced fasting plasma glucose levels, increased triglycerides levels and lower HOMA-IR in Japanese population.
|
20574426 |
2010 |
|
rs17145738
|
|
C |
0.710 |
GeneticVariation |
GWASCAT |
A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.
|
27599772 |
2017 |
|
rs17145738
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Variants more frequently identified in isolated hypertriglyceridemias were rs7412 in APOE and rs1800795 in IL6; rs2808607 in CYP7A1 and rs3812316 and rs17145738 in MLXIPL were more frequent in FCHL.
|
25176936 |
2014 |
|
rs10808546
|
|
C |
0.700 |
GeneticVariation |
GWASCAT |
A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.
|
27599772 |
2017 |
|
rs10911205
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.
|
27599772 |
2017 |
|
rs10911232
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.
|
27599772 |
2017 |