Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4986790
rs4986790
0.020 GeneticVariation BEFREE Genomic Analysis of Single Nucleotide Polymorphisms Asp299Gly and Thr399Ile in Japanese Patients with Invasive Aspergillosis. 25766605

2015

dbSNP: rs4986791
rs4986791
0.020 GeneticVariation BEFREE Genomic Analysis of Single Nucleotide Polymorphisms Asp299Gly and Thr399Ile in Japanese Patients with Invasive Aspergillosis. 25766605

2015

dbSNP: rs4986790
rs4986790
0.020 GeneticVariation BEFREE We analyzed 154 patients after allogeneic HSCT for acute leukemia for TLR4 gene variants 1063A/G (D299G) and 1363C/T (T399I) with their respective donors, and correlated the results with the incidence of invasive aspergillosis (IA) infection after transplant. 23890253

2013

dbSNP: rs4986791
rs4986791
0.020 GeneticVariation BEFREE We analyzed 154 patients after allogeneic HSCT for acute leukemia for TLR4 gene variants 1063A/G (D299G) and 1363C/T (T399I) with their respective donors, and correlated the results with the incidence of invasive aspergillosis (IA) infection after transplant. 23890253

2013

dbSNP: rs16910526
rs16910526
0.020 GeneticVariation BEFREE Dectin-1 Y238X heterozygosity has a limited influence on susceptibility to IA and may be important in susceptible non-HSCT patients. 21242599

2011

dbSNP: rs16910526
rs16910526
0.020 GeneticVariation BEFREE Dectin-1 Y238X polymorphism associates with susceptibility to invasive aspergillosis in hematopoietic transplantation through impairment of both recipient- and donor-dependent mechanisms of antifungal immunity. 20807886

2010

dbSNP: rs1616583
rs1616583
0.010 GeneticVariation BEFREE To clarify the potential involvement of two novel single-nucleotide polymorphisms (SNPs) located in the <i>TLR7</i> gene (rs1634318 and rs1616583) in a variety of immune-related conditions, we studied the variability of these loci in patients from a Polish population with SLE and DLE, as well as in immunocompromised patients who were affected by invasive aspergillosis (IA) and those who were not affected. 29599669

2018

dbSNP: rs5744168
rs5744168
0.010 GeneticVariation BEFREE While no association was found for donor SNPs and the recipients' risk of IA, analysis of recipient SNPs showed a significant association between the presence of recipient TLR5-Stop SNP (1174C> T) and the incidence of IA (P = 0.004). 23862689

2013

dbSNP: rs778657916
rs778657916
0.010 GeneticVariation BEFREE While no association was found for donor SNPs and the recipients' risk of IA, analysis of recipient SNPs showed a significant association between the presence of recipient TLR5-Stop SNP (1174C> T) and the incidence of IA (P = 0.004). 23862689

2013

dbSNP: rs334558
rs334558
0.010 GeneticVariation BEFREE Screening of patients after allogeneic stem cell transplantation (with or without IA) for the presence of genetic markers (rs334558, rs6438552) in the GSK-3 gene revealed no significant association with an increased risk for IA. 20055739

2010

dbSNP: rs6438552
rs6438552
0.010 GeneticVariation BEFREE Screening of patients after allogeneic stem cell transplantation (with or without IA) for the presence of genetic markers (rs334558, rs6438552) in the GSK-3 gene revealed no significant association with an increased risk for IA. 20055739

2010

dbSNP: rs1371329921
rs1371329921
0.010 GeneticVariation BEFREE Analysis of recipient SNP data showed that the presence of TLR1 239G > C (Arg80 > Thr) or the presence of both TLR1 743A > G (Asn248 > Ser) and TLR6 745C > T (Ser249 > Pro) is associated with IA (odds ratio = 1.30, 95% confidence interval = 1.13 to 1.50; P < .001). 16461792

2005

dbSNP: rs4833095
rs4833095
0.010 GeneticVariation BEFREE Analysis of recipient SNP data showed that the presence of TLR1 239G > C (Arg80 > Thr) or the presence of both TLR1 743A > G (Asn248 > Ser) and TLR6 745C > T (Ser249 > Pro) is associated with IA (odds ratio = 1.30, 95% confidence interval = 1.13 to 1.50; P < .001). 16461792

2005

dbSNP: rs5743611
rs5743611
0.010 GeneticVariation BEFREE Analysis of recipient SNP data showed that the presence of TLR1 239G > C (Arg80 > Thr) or the presence of both TLR1 743A > G (Asn248 > Ser) and TLR6 745C > T (Ser249 > Pro) is associated with IA (odds ratio = 1.30, 95% confidence interval = 1.13 to 1.50; P < .001). 16461792

2005

dbSNP: rs5743810
rs5743810
0.010 GeneticVariation BEFREE Analysis of recipient SNP data showed that the presence of TLR1 239G > C (Arg80 > Thr) or the presence of both TLR1 743A > G (Asn248 > Ser) and TLR6 745C > T (Ser249 > Pro) is associated with IA (odds ratio = 1.30, 95% confidence interval = 1.13 to 1.50; P < .001). 16461792

2005

dbSNP: rs775910328
rs775910328
0.010 GeneticVariation BEFREE Analysis of recipient SNP data showed that the presence of TLR1 239G > C (Arg80 > Thr) or the presence of both TLR1 743A > G (Asn248 > Ser) and TLR6 745C > T (Ser249 > Pro) is associated with IA (odds ratio = 1.30, 95% confidence interval = 1.13 to 1.50; P < .001). 16461792

2005