rs2681472
|
|
|
0.860 |
GeneticVariation |
BEFREE |
Recently STK39 rs3754777, ATP2B1 rs2681472 and rs17249754 have been associated with BP variation and hypertension.
|
31242870 |
2019 |
rs2681472
|
|
A |
0.860 |
GeneticVariation |
GWASCAT |
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.
|
30487518 |
2018 |
rs2681472
|
|
|
0.860 |
GeneticVariation |
BEFREE |
The aim of this study was to assess the associations of <i>ATP2B1</i> rs2681472 and <i>CACNB2</i> rs12258967 gene polymorphisms with high blood pressure (HBP) among Lithuanian children and adolescents aged 12-15 years.
|
29982197 |
2018 |
rs2681472
|
|
|
0.860 |
GeneticVariation |
BEFREE |
Recently, a genome-wide association study (GWAS) identified the single-nucleotide polymorphism, rs2681472, as a new hypertension susceptibility genetic variant.
|
24642721 |
2014 |
rs2681472
|
|
|
0.860 |
GeneticVariation |
BEFREE |
The major findings of this study were that four loci--rs10858911, rs2681472, rs17249754 and rs1401982--associated with any or all of four traits: hypertension (P = 0.001-4.6E-05; odds ratio, 0.83-0.87), systolic BP (P = 0.003-0.004), diastolic BP (P = 0.002-0.003) and cf-PWV (P = 0.002-0.004).
|
23079715 |
2013 |
rs2681472
|
|
|
0.860 |
GeneticVariation |
BEFREE |
Association of allelic variants in rs2681472 and rs2681492 with hypertension, rs987237 and rs7826222 with waist circumference and rs864745, rs7578597 and rs2943641 with diabetes were not significant.
|
23036851 |
2013 |
rs2681472
|
|
|
0.860 |
GeneticVariation |
BEFREE |
The results suggested that rs2681472 was significantly associated with hypertension risk in East Asians (OR = 1.18, 95% CI 1.10-1.27, p = 0.000).
|
22229515 |
2012 |
rs2681472
|
|
A |
0.860 |
GeneticVariation |
GWASCAT |
Genome-wide association study of blood pressure and hypertension.
|
19430479 |
2009 |
rs2681472
|
|
A |
0.860 |
GeneticVariation |
GWASDB |
Genome-wide association study of blood pressure and hypertension.
|
19430479 |
2009 |
rs1799945
|
|
|
0.840 |
GeneticVariation |
BEFREE |
Compared with WT/WT, H63D</span>/WT and H63D</span>/H6</span>3D participants had a 2% to 4% and 4% to 7% absolute increase in hypertension risk at each visit, respectively.
|
30571559 |
2019 |
rs1799945
|
|
|
0.840 |
GeneticVariation |
BEFREE |
According to GWAS studies, iron regulatory protein HFE gene variant H63D (rs1799945) was associated with hypertension, an observation which we were able to confirm also in our TAMRISK cohort.
|
28151915 |
2017 |
rs1799945
|
|
|
0.840 |
GeneticVariation |
BEFREE |
We found that individuals with the mutated form of the H63D polymorphic site (G-allele) had a 1.4-fold risk (P = 0.037, 95% confidence interval [CI] 1.02-1.89) for hypertension at the age of 50 years compared with the CC genotype carriers.
|
25634189 |
2015 |
rs1799945
|
|
|
0.840 |
GeneticVariation |
BEFREE |
Multivariate analysis revealed that the odds of CHF was higher in females [Odds Ratio (OR) = 2·9, P < 0·01], individuals with pre-HCT chest radiation (OR = 4·7, P = 0·05), hypertension (OR = 2·9, P = 0·01), and with variants of genes coding for the NAD(P)H-oxidase subunit RAC2 (rs13058338, 7508T→A; OR = 2·8, P < 0·01), HFE (rs1799945, 63C→G; OR = 2·5, P = 0·05) or the doxorubicin efflux transporter ABCC2 (rs8187710, 1515G→A; OR = 4·3, P < 0·01).
|
23927520 |
2013 |
rs1799945
|
|
G |
0.840 |
GeneticVariation |
GWASDB |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
21909115 |
2011 |
rs1799945
|
|
G |
0.840 |
GeneticVariation |
GWASCAT |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
21909115 |
2011 |
rs13333226
|
|
A |
0.810 |
GeneticVariation |
GWASCAT |
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
|
27618447 |
2016 |
rs2932538
|
|
|
0.810 |
GeneticVariation |
BEFREE |
SNP rs2932538, a variant in MOV10, was found to be significantly associated with an increased risk of hypertension.
|
24338417 |
2013 |
rs4373814
|
|
|
0.810 |
GeneticVariation |
BEFREE |
However, SNP rs4373814, a variant in CACNB2, showed a relevant association with a decreased risk of hypertension.
|
24338417 |
2013 |
rs6596140
|
|
T |
0.810 |
GeneticVariation |
GWASDB |
Using a family-based association test, we found an association with SNPs on chromosome 5q31.1 (rs6596140; P<9 × 10(-8)) for hypertension.
|
22384028 |
2012 |
rs6596140
|
|
|
0.810 |
GeneticVariation |
BEFREE |
Using a family-based association test, we found an association with SNPs on chromosome 5q31.1 (rs6596140; P<9 × 10(-8)) for hypertension.
|
22384028 |
2012 |
rs6596140
|
|
T |
0.810 |
GeneticVariation |
GWASCAT |
Using a family-based association test, we found an association with SNPs on chromosome 5q31.1 (rs6596140; P<9 × 10(-8)) for hypertension.
|
22384028 |
2012 |
rs2932538
|
|
G |
0.810 |
GeneticVariation |
GWASDB |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
21909115 |
2011 |
rs2932538
|
|
G |
0.810 |
GeneticVariation |
GWASCAT |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
21909115 |
2011 |
rs4373814
|
|
G |
0.810 |
GeneticVariation |
GWASDB |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
21909115 |
2011 |
rs4373814
|
|
G |
0.810 |
GeneticVariation |
GWASCAT |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
21909115 |
2011 |