rs587782477
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To clarify the mechanism underlying these observations we have developed a model of lung inflammation using adoptively transferred CD4(+) T cells expressing a Valpha11(+)Vbeta3(+) transgenic TCR specific for I-E(k) and moth cytochrome c. Treatment with Y100F-Ig inhibited the induction of lung eosinophilia in adoptively transferred mice.
|
11290768 |
2001 |
rs2294021
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The relationships between FOXP3 rs3761547, rs3761548, rs3761549, rs2232365, rs2280883, and CCDC22 rs2294021 polymorphisms and clinical outcomes such as acute rejection, TAC-induced acute nephrotoxicity, and pneumonia were investigated by using Kaplan-Meier estimates and multivariate Cox regression analysis.
|
27747372 |
2017 |
rs1217371203
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To clarify the mechanism underlying these observations we have developed a model of lung inflammation using adoptively transferred CD4(+) T cells expressing a Valpha11(+)Vbeta3(+) transgenic TCR specific for I-E(k) and moth cytochrome c. Treatment with Y100F-Ig inhibited the induction of lung eosinophilia in adoptively transferred mice.
|
11290768 |
2001 |
rs113993959
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs74597325
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs213950
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Caucasian and African American children with pneumonia were genotyped for the most common variants reported to affect cystic fibrosis transmembrane conductance regulator function, the p.508del mutation, the (TG)mTn variable repeat region, and the M470V polymorphism in the cystic fibrosis transmembrane conductance regulator gene.
|
22890249 |
2012 |
rs7309123
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We could demonstrate that patients carrying the Dectin-1 SNP rs7309123 G/G (n = 47) or G/G and C/G (n = 133) genotype revealed a significant higher risk for developing both pneumonia in general (adjusted odds ratio (OR): 2.5; p = 0.014 and OR: 3.0, p = 0.004) and pulmonary IFD (OR: 2.6; p = 0.012 and OR: 2.4, p = 0.041, respectively).
|
26963509 |
2016 |
rs17615
|
|
|
0.010 |
GeneticVariation |
BEFREE |
One patient had 3 homozygous nonsynonymous variations of the complement receptor 2 (CR2) gene distributed in exons 10 (c.1916G>A, p.S639N) and 11 (c.1987T>C, p.S663P and c.2012G>A, p.R671H) with high frequency.This case series suggests that fungi are important respiratory pathogens in children with HIES and should be considered in cases of pneumonia in this population.
|
29620631 |
2018 |
rs17616
|
|
|
0.010 |
GeneticVariation |
BEFREE |
One patient had 3 homozygous nonsynonymous variations of the complement receptor 2 (CR2) gene distributed in exons 10 (c.1916G>A, p.S639N) and 11 (c.1987T>C, p.S663P and c.2012G>A, p.R671H) with high frequency.This case series suggests that fungi are important respiratory pathogens in children with HIES and should be considered in cases of pneumonia in this population.
|
29620631 |
2018 |
rs4308977
|
|
|
0.010 |
GeneticVariation |
BEFREE |
One patient had 3 homozygous nonsynonymous variations of the complement receptor 2 (CR2) gene distributed in exons 10 (c.1916G>A, p.S639N) and 11 (c.1987T>C, p.S663P and c.2012G>A, p.R671H) with high frequency.This case series suggests that fungi are important respiratory pathogens in children with HIES and should be considered in cases of pneumonia in this population.
|
29620631 |
2018 |
rs4957796
|
|
|
0.710 |
GeneticVariation |
GWASCAT |
Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study.
|
25533491 |
2015 |
rs4957796
|
|
|
0.710 |
GeneticVariation |
BEFREE |
In conclusion, FER rs4957796 might act as a prognostic variable for survival in patients with severe ARDS due to pneumonia.
|
28851893 |
2017 |
rs1057520529
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs601338
|
|
|
0.010 |
GeneticVariation |
BEFREE |
For FUT2 SNP rs601338, the risk ratios for ≥1 bout of diarrhea during ages 6-12 months and ages 12-24 months per additional risk (G) allele were 1.23 (95% confidence interval [CI], 1.08-1.4; P = .002) and 1.41 (95% CI, 1.24-1.61; P = 1.7 × 10-7), respectively; the risk ratio for ≥1 diagnosis of a lower respiratory illness (ie, pneumonia or bronchiolitis) during ages 12-24 months per additional G allele was 2.66 (95% CI, 1.64-4.3; P = .00007).
|
30376117 |
2019 |
rs796051877
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
c.1437G>A intron 9 substitution on acid α-glucosidase gene associated with classic infantile-onset Pompe disease phenotype.
|
26160551 |
2015 |
rs1045411
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To investigate the relationship between the high mobility group box protein B1 (HMGB1) single nucleotide polymorphisms (SNPs) rs1412125, rs2249825, and rs1045411 with pneumonia in terms of susceptibility, severity, and inflammatory response.
|
30562142 |
2019 |
rs1412125
|
|
|
0.010 |
GeneticVariation |
BEFREE |
SNPs at the rs1412125 and rs2249825 loci of HMGB1 are associated with pneumonia in terms of susceptibility, severity, and inflammatory response.
|
30562142 |
2019 |
rs2249825
|
|
|
0.010 |
GeneticVariation |
BEFREE |
SNPs at the rs1412125 and rs2249825 loci of HMGB1 are associated with pneumonia in terms of susceptibility, severity, and inflammatory response.
|
30562142 |
2019 |
rs12252
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We have genotyped a possible splice-site altering single-nucleotide polymorphism (rs12252) in the IFITM3 gene in 34 patients with H1N1 influenza and severe pneumonia, and >5000 individuals comprising patients with community-acquired mild lower respiratory tract infection and matched controls of Caucasian ancestry.
|
23997235 |
2014 |
rs4251961
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Higher plasma IL-1ra was associated with an increased risk of infection (other than pneumonia), and the minor C allele of rs4251961 was independently associated with a decreased risk of infection (other than pneumonia).
|
24233813 |
2014 |
rs1800795
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In intensive care unit patients, the TNF-α -308A allele and the IL-6 rs1800795 allele variants were susceptibility risk factors for septic shock induced by pneumonia.
|
26025100 |
2015 |
rs879253740
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1131692245
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1130866
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Previous studies have indicated that a SP-B 1580C/T polymorphism (SNP rs1130866) was associated with lung diseases including pneumonia.
|
26620227 |
2016 |
rs1057518731
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|