|
rs763780
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Assessment of IL-17F rs763780 gene polymorphism in immune thrombocytopenia.
|
30594845 |
2019 |
|
rs763780
|
|
|
0.020 |
GeneticVariation |
BEFREE |
In conclusion, IL-17F rs763780 polymorphisms may be associated with the development of ITP in a Chinese Han population.
|
26620416 |
2017 |
|
rs153109
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Our results indicate that the genetic polymorphisms of IL-27 rs153109 and rs181206 may be involved in the progression of human cancers and diseases, especially of TB, UC, COPD, OC, and ITP.
|
26950245 |
2016 |
|
rs1884444
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Interleukin-23 receptor rs1884444 single nucleotide polymorphism was studied in 50 patients with primary immune thrombocytopenia and 100 healthy age and sex-matched controls by polymerase chain reaction amplification of the target gene followed by allele-specific restriction enzyme digestion.
|
26859125 |
2016 |
|
rs2297630
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Stromal cell-derived factor-1 rs2297630 polymorphism associated with platelet production and treatment response in Chinese patients with chronic immune thrombocytopenia.
|
26587874 |
2016 |
|
rs153109
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Interleukin-27 rs153109 polymorphism and the risk for immune thrombocytopenia.
|
23937109 |
2013 |
|
rs1884444
|
|
|
0.020 |
GeneticVariation |
BEFREE |
This study suggests that polymorphism in the IL-23R gene, rs1884444, indicates a significant association with susceptibility to ITP in a recessive genetic model but does not have association with the clinical outcome of HD-DXM therapy.
|
23564312 |
2013 |
|
rs2297630
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Further analysis of the relationship between SDF-1 polymorphisms and clinical features showed that rs2297630 A/G was associated with protection from chronicity (P = 0.002; OR, 0.07; 95% CI, 0.01-0.61) and steroid dependence (P = 0.007; OR, 0.10; 95% CI, 0.01-0.84) in ITP patients.
|
23078136 |
2013 |
|
rs2501432
|
|
|
0.020 |
GeneticVariation |
BEFREE |
There was a significant statistical difference in the distribution of CNR2 Q63R genotypes between chronic ITP patients group and the control groups.
|
23406660 |
2013 |
|
rs35761398
|
|
|
0.020 |
GeneticVariation |
BEFREE |
There was a significant statistical difference in the distribution of CNR2 Q63R genotypes between chronic ITP patients group and the control groups.
|
23406660 |
2013 |
|
rs879761216
|
|
|
0.020 |
GeneticVariation |
BEFREE |
There was a significant statistical difference in the distribution of CNR2 Q63R genotypes between chronic ITP patients group and the control groups.
|
23406660 |
2013 |
|
rs2501432
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We evaluated a common missense variant (CAA/CGG; Q63R) of the gene encoding the cannabinoid receptor type 2 (GeneID 1269) in 190 children with immune thrombocytopenic purpura and 600 healthy controls.
|
21828121 |
2011 |
|
rs35761398
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We evaluated a common missense variant (CAA/CGG; Q63R) of the gene encoding the cannabinoid receptor type 2 (GeneID 1269) in 190 children with immune thrombocytopenic purpura and 600 healthy controls.
|
21828121 |
2011 |
|
rs879761216
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We evaluated a common missense variant (CAA/CGG; Q63R) of the gene encoding the cannabinoid receptor type 2 (GeneID 1269) in 190 children with immune thrombocytopenic purpura and 600 healthy controls.
|
21828121 |
2011 |
|
rs1050501
|
|
|
0.010 |
GeneticVariation |
BEFREE |
But we did not observe any significant associations with ITP for FCGR2A H131R and FCGR2B I232T polymorphisms in overall analyses.
|
30786049 |
2019 |
|
rs1308699981
|
|
|
0.010 |
GeneticVariation |
BEFREE |
But we did not observe any significant associations with ITP for FCGR2A H131R and FCGR2B I232T polymorphisms in overall analyses.
|
30786049 |
2019 |
|
rs2430561
|
|
|
0.010 |
GeneticVariation |
BEFREE |
rs2430561 does not seem to have any role in ITP pathogenesis and treatment response.
|
30955035 |
2019 |
|
rs4077515
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, CARD9 rs4077515 polymorphism had no effect on corticosteroid sensitivity or refractoriness of IT</span>P.
|
31595308 |
2019 |
|
rs77375493
|
|
|
0.010 |
GeneticVariation |
BEFREE |
JAK2 V617F-positive essential thrombocythemia with subsequent development of immune thrombocytopenia: A case report.
|
31689837 |
2019 |
|
rs745738344
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The potential association of tumor necrosis factor-βeta (252 G/A) cytokine gene polymorphism with immune thrombocytopenic purpura among Egyptian children.
|
29020887 |
2018 |
|
rs10499194
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings suggest that rs10499194 may be a protective factor for susceptibility and corticosteroid sensitivity in ITP patients.
|
28702029 |
2017 |
|
rs1161169998
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Conclusion p.G76S mutation on the TNFRSF13B gene is responsible for ITP, and is a genetic predisposing factor for familial or sporadic ITP.
|
28834165 |
2017 |
|
rs146436713
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Conclusion p.G76S mutation on the TNFRSF13B gene is responsible for ITP, and is a genetic predisposing factor for familial or sporadic ITP.
|
28834165 |
2017 |
|
rs1883832
|
|
|
0.010 |
GeneticVariation |
BEFREE |
CD40 rs1883832 is associated with decreased risk of Graves' disease, especially in Asian; CD40 rs1883832 is associated with increased risk of multiple sclerosis; CD40 -1C>T (rs1883832) is not associated with the susceptibility of Hashimoto's thyroiditis, systemic sclerosis or Asthma; there is insufficient data to fully confirm the association between CD40 rs1883832 and systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), Behçet's disease (BD), myasthenia gravis (MG), Crohn's disease (CD), ulcerative colitis (UC), Sarcoidosis, Fuch uveitis syndrome (FUS), Vogt-Koyanagi-Harada syndrome (VKH), Kawasaki disease (KD), giant cell arteritis (GCA) or Immune thrombocytopenia (ITP).
|
29254239 |
2017 |
|
rs200215055
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The FCGR3A (158V/F) polymorphism, known to increase the affinity of FcγRIII to IgG, was over-represented in ITP patients.
|
28142207 |
2017 |