|
Triglycerides measurement
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
|
28548082 |
2017 |
|
VLDL cholesterol measurement
|
|
0.700 |
GeneticVariation
|
GWASCAT |
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
|
28548082 |
2017 |
|
Dyslipidemias
|
|
0.020 |
GeneticVariation
|
BEFREE |
We also demonstrate that rs964184 has a large effect (odds ratio, 1.74) and is more frequent in the Mexican population, and thus it may contribute to the high predisposition to dyslipidemias in Mexicans.
|
20160193 |
2010 |
|
Triglycerides measurement
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.
|
31560688 |
2019 |
|
Dyslipidemias
|
|
0.020 |
GeneticVariation
|
BEFREE |
There were significant associations between rs1260333 (OR is 0.82, 95 % CI 0.74-0.92, p ~ 3.96 × 10(-4)), rs1260326 (OR is 0.82, 95 % CI 0.74-0.92, p ~ 5.31 × 10(-4)), and rs964184 (OR is 1.36, 95 % CI 1.20-1.55, p ~ 1.89 × 10(-6)) and dyslipidemia.
|
23832694 |
2013 |
|
Hypochondroplasia (disorder)
|
|
0.010 |
GeneticVariation
|
BEFREE |
The ZNF259 rs2075290, ZNF259 rs964184</span> and BUD13 rs10790162 SNPs were significantly associated with serum lipid levels in both HCH and non-HCH populations (P < 0.008-0.001).
|
24780069 |
2014 |
|
High density lipoprotein measurement
|
|
0.800 |
GeneticVariation
|
GWASCAT |
The impact of low-frequency and rare variants on lipid levels.
|
25961943 |
2015 |
|
Triglycerides measurement
|
|
0.800 |
GeneticVariation
|
GWASCAT |
The impact of low-frequency and rare variants on lipid levels.
|
25961943 |
2015 |
|
Low density lipoprotein cholesterol measurement
|
|
0.800 |
GeneticVariation
|
GWASCAT |
The impact of low-frequency and rare variants on lipid levels.
|
25961943 |
2015 |
|
Serum total cholesterol measurement
|
|
0.800 |
GeneticVariation
|
GWASCAT |
The impact of low-frequency and rare variants on lipid levels.
|
25961943 |
2015 |
|
Anemia, Sickle Cell
|
|
0.010 |
GeneticVariation
|
BEFREE |
The G-risk allele rs964184/ZPRI ZNF259/ZPR1 gene (GC + GG genotypes) was associated with increased levels of TG in children ≥10 years old (p = 0.045) and the atherogenic ratio TG/HDL-C (p = 0.032) in SCD.
|
31670185 |
2020 |
|
Hypertriglyceridemia
|
|
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 |
|
Prostate carcinoma
|
|
0.010 |
GeneticVariation
|
BEFREE |
The association between rs964184 and prostate cancer risk was stronger among homozygous carriers of the minor allele (OR = 0.27; 95% CI: 0.09, 0.83).
|
24623848 |
2014 |
|
Malignant neoplasm of prostate
|
|
0.010 |
GeneticVariation
|
BEFREE |
The association between rs964184 and prostate cancer risk was stronger among homozygous carriers of the minor allele (OR = 0.27; 95% CI: 0.09, 0.83).
|
24623848 |
2014 |
|
Reticulocyte count (procedure)
|
|
0.700 |
GeneticVariation
|
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
Platelet Component Distribution Width Measurement
|
|
0.700 |
GeneticVariation
|
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
RDW - Red blood cell distribution width result
|
|
0.700 |
GeneticVariation
|
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
Corpuscular Hemoglobin Concentration Mean
|
|
0.700 |
GeneticVariation
|
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
Red cell distribution width determination
|
|
0.700 |
GeneticVariation
|
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
Platelet mean volume determination (procedure)
|
|
0.700 |
GeneticVariation
|
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
Cardiovascular Diseases
|
|
0.710 |
GeneticVariation
|
BEFREE |
The 11q23.3 genomic region-rs964184-is associated with cardiovascular disease in patients with rheumatoid arthritis.
|
24131021 |
2013 |
|
Hypertriglyceridemia
|
|
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 |
|
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 |
|
Coronary heart disease
|
|
0.830 |
GeneticVariation
|
BEFREE |
Recently, the rs964184 polymorphism has been associated with coronary artery disease in nonrheumatic Caucasian individuals.
|
24131021 |
2013 |
|
Coronary Artery Disease
|
|
0.730 |
GeneticVariation
|
BEFREE |
Recently, the rs964184 polymorphism has been associated with coronary artery disease in nonrheumatic Caucasian individuals.
|
24131021 |
2013 |