Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4986790
rs4986790
0.090 GeneticVariation BEFREE The aim of this study was to investigate the possible role of polymorphisms of TLR4, Asp299Gly and Thr399Ile and CD14, C-159T and C-550T in the development of RSV bronchiolitis. 25572736

2015

dbSNP: rs4986790
rs4986790
0.090 GeneticVariation BEFREE The TLR4 (Asp299Gly), TLR4 (Thr399Ile), and JUN (c.750G/A) SNPs showed no significant association with RSV disease. 21837802

2011

dbSNP: rs4986790
rs4986790
0.090 GeneticVariation BEFREE TLR4 Asp299Gly and Thr399Ile polymorphisms: no impact on human immune responsiveness to LPS or respiratory syncytial virus. 20711470

2010

dbSNP: rs4986790
rs4986790
0.090 GeneticVariation BEFREE The aim was to study the association between the TLR4 Asp299Gly polymorphism and the susceptibility to severe RSV bronchiolitis in infants. 20575099

2010

dbSNP: rs4986790
rs4986790
0.090 GeneticVariation BEFREE By genotyping 236 children with RSV infection and 219 healthy controls we found no association between the risk of severe RSV infection and Asp299Gly polymorphisms (P>0.05), and we demonstrate that the TLR4 Asp299Gly genotype does not influence susceptibility to either RSV serotype A or B (P>0.05). 17449325

2007

dbSNP: rs4986790
rs4986790
0.090 GeneticVariation BEFREE Both SNPs were highly associated with symptomatic RSV disease in this largely premature population (p < 0.0001), with 89.5% and 87.6% of cases being heterozygous for Asp299Gly and Thr399Ile polymorphisms versus published control frequencies of 10.5% and 6.5%, respectively. 17709532

2007

dbSNP: rs4986790
rs4986790
0.090 GeneticVariation BEFREE The presence of TLR4 mutations (Asp299Gly and Thr399Ile) were associated with severe RSV bronchiolitis and were significantly over-represented in groups II and III. 16542364

2006

dbSNP: rs4986790
rs4986790
0.090 GeneticVariation BEFREE We genotyped the CD14 promotor polymorphism -C159T and the two common TLR4 amino acid variants (D259G, and T359I) in 131 infants with severe RSV associated diseases and 270 controls. 17264400

2006

dbSNP: rs4986790
rs4986790
0.090 GeneticVariation BEFREE The association of the TLR4 mutations (Asp299Gly and Thr399Ile) and the CD14/-159 polymorphism were analyzed in 99 infants hospitalized with severe RSV bronchiolitis (group I). 15143473

2004

dbSNP: rs4986791
rs4986791
0.070 GeneticVariation BEFREE The aim of this study was to investigate the possible role of polymorphisms of TLR4, Asp299Gly and Thr399Ile and CD14, C-159T and C-550T in the development of RSV bronchiolitis. 25572736

2015

dbSNP: rs4986791
rs4986791
0.070 GeneticVariation BEFREE The TLR4 (Asp299Gly), TLR4 (Thr399Ile), and JUN (c.750G/A) SNPs showed no significant association with RSV disease. 21837802

2011

dbSNP: rs4986791
rs4986791
0.070 GeneticVariation BEFREE TLR4 Asp299Gly and Thr399Ile polymorphisms: no impact on human immune responsiveness to LPS or respiratory syncytial virus. 20711470

2010

dbSNP: rs4986791
rs4986791
0.070 GeneticVariation BEFREE Both SNPs were highly associated with symptomatic RSV disease in this largely premature population (p < 0.0001), with 89.5% and 87.6% of cases being heterozygous for Asp299Gly and Thr399Ile polymorphisms versus published control frequencies of 10.5% and 6.5%, respectively. 17709532

2007

dbSNP: rs4986791
rs4986791
0.070 GeneticVariation BEFREE The presence of TLR4 mutations (Asp299Gly and Thr399Ile) were associated with severe RSV bronchiolitis and were significantly over-represented in groups II and III. 16542364

2006

dbSNP: rs4986791
rs4986791
0.070 GeneticVariation BEFREE We genotyped the CD14 promotor polymorphism -C159T and the two common TLR4 amino acid variants (D259G, and T359I) in 131 infants with severe RSV associated diseases and 270 controls. 17264400

2006

dbSNP: rs4986791
rs4986791
0.070 GeneticVariation BEFREE The association of the TLR4 mutations (Asp299Gly and Thr399Ile) and the CD14/-159 polymorphism were analyzed in 99 infants hospitalized with severe RSV bronchiolitis (group I). 15143473

2004

dbSNP: rs757275190
rs757275190
0.010 GeneticVariation BEFREE We show that infection of polarized Calu3 respiratory cells with recombinant RSV having point mutations in Cys173 and 176 (C173/176S) (rA2-GC12), or Cys186 (C186S) (rA2-GC4) is associated with a decline in the integrity of polarized Calu-3 cultures and decreased virus production. 28671606

2017

dbSNP: rs1800888
rs1800888
0.010 GeneticVariation BEFREE One of the variants was a highly functional nonsynonymous variant in ADRB2 (rs1800888), which was also nominally associated with asthma (p = 0.027) and active asthma (p = 0.013) among European Americans with severe RSV bronchiolitis without including the ESP. 26587832

2015

dbSNP: rs3138557
rs3138557
0.010 GeneticVariation BEFREE The aim of this study was to investigate whether IFN-γ CA microsatellite (rs3138557) polymorphism was associated with susceptibility to RSV in Chinese Han children and with the severity of the infection. 25130433

2014

dbSNP: rs4588
rs4588
GC
0.010 GeneticVariation BEFREE We assessed the relationship between polymorphisms rs7041 and rs4588, which define haplotypes GC1s, GC1f, and GC2, and RSV bronchiolitis susceptibility and subsequent asthma. 24447085

2014

dbSNP: rs7041
rs7041
GC
0.010 GeneticVariation BEFREE The rs7041_C allele was also more frequent in the RSV bronchiolitis group compared with controls (OR 1.12, 95% CI 1.02, 1.4, P = 0.03) in the Netherlands, especially in mechanically ventilated patients (P = 0.009). 24447085

2014

dbSNP: rs1799971
rs1799971
0.010 GeneticVariation BEFREE In our human study, the A118G single nucleotide polymorphism rs1799971 was associated with respiratory syncytial virus disease severity (p = 0.015). 23222260

2013

dbSNP: rs4543123
rs4543123
0.010 GeneticVariation BEFREE The TLR1 variant (rs4543123) was associated with both multiple viruses (respiratory syncytial virus and parainfluenza virus) and multiple phenotypes. 23063165

2012

dbSNP: rs1799962
rs1799962
IL9
0.010 GeneticVariation BEFREE Haplotype analysis of two SNPs in the IL-9 gene (rs2069885 and rs1799962) showed overrepresentation of the TT haplotype in girls with severe RSV bronchiolitis requiring hospitalization indicating that this is the haplotype conferring the highest risk in girls. 20503287

2010

dbSNP: rs2069885
rs2069885
IL9
0.010 GeneticVariation BEFREE Haplotype analysis of two SNPs in the IL-9 gene (rs2069</span>885 and rs1799962) showed overrepresentation of the TT haplotype in girls with severe RSV bronchiolitis requiring hospitalization indicating that this is the haplotype conferring the highest risk in girls. 20503287

2010