|
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 |