Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801274
rs1801274
0.010 GeneticVariation BEFREE The functional single nucleotide polymorphism rs1801274 in the FCGR2A gene (His131Arg) influences the efficiency of hIgG2 binding, the main isotype produced in response to encapsulated bacteria like Streptococcus pneumoniae and Haemophilus influenzae. 16893392

2006

dbSNP: rs4986791
rs4986791
0.020 GeneticVariation BEFREE On the contrary, the presence of the TLR4-T399I polymorphism was associated with a 2-fold decreased risk of Haemophilus influenzae carriage (OR = 0.38, 95% CI = 0.15 to 0.96, P = 0.038). 21159925

2011

dbSNP: rs773340854
rs773340854
0.010 GeneticVariation BEFREE On the contrary, the presence of the TLR4-T399I polymorphism was associated with a 2-fold decreased risk of Haemophilus influenzae carriage (OR = 0.38, 95% CI = 0.15 to 0.96, P = 0.038). 21159925

2011

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE We find that a statistically significant number of hospitalized subjects show enrichment for a minor IFITM3 allele (SNP rs12252-C) that alters a splice acceptor site, and functional assays show the minor CC genotype IFITM3 has reduced influenza virus restriction in vitro. 22446628

2012

dbSNP: rs2229291
rs2229291
0.010 GeneticVariation BEFREE Recent studies suggested that the thermolabile phenotype of carnitine palmitoyltransferase II (CPT II) variation [F352C] was closely related to the pathomechanism of influenza-associated encephalopathy (IAE) in Japanese, causing mitochondrial ATP utilization failure during periods of high fever, resulting in brain edema. 21277129

2012

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE Interferon-induced transmembrane protein-3 genetic variant rs12252-C is associated with severe influenza in Chinese individuals. 23361009

2013

dbSNP: rs4986791
rs4986791
0.020 GeneticVariation BEFREE TLR4 1196 C>T effects were similar to TLR4 896 A>G for brucellosis, cutaneous leishmaniasis, leprosy, typhoid fever and S. pyogenes tonsillar disease, and was protective for bacterial vaginosis in pregnancy (0.55; 95%CI 0.31-0.98) and Haemophilus influenzae tonsillar disease (0.42; 95%CI 0.17-1.00). 24282567

2013

dbSNP: rs1468575151
rs1468575151
0.010 GeneticVariation BEFREE We found a novel mutation, N84S in the PB1F2 protein of 9·35% of the highly pathogenic avian influenza H5N1 influenza viruses. 22788742

2013

dbSNP: rs7744020
rs7744020
0.010 GeneticVariation BEFREE Variants in the Human Leukocyte Antigen (HLA)- DQ region were associated with age of onset (rs7744020 P = 7.9×10(-9) beta -1.9 years) and varied significantly among cases with onset after the 2009 H1N1 influenza pandemic compared to previous years (rs9271117 P = 7.8 × 10(-10) OR 0.57). 24204295

2013

dbSNP: rs9271117
rs9271117
0.010 GeneticVariation BEFREE Variants in the Human Leukocyte Antigen (HLA)- DQ region were associated with age of onset (rs7744020 P = 7.9×10(-9) beta -1.9 years) and varied significantly among cases with onset after the 2009 H1N1 influenza pandemic compared to previous years (rs9271117 P = 7.8 × 10(-10) OR 0.57). 24204295

2013

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE We found evidence of an association between rs12252 rare allele homozygotes and susceptibility to mild influenza (in patients attending primary care) but could not confirm a previously reported association between this single-nucleotide polymorphism and susceptibility to severe H1N1 infection. 23997235

2014

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE They also suggested that mechanisms, other than viral entry restriction, might contribute to variations in clinical outcomes of H1N1 influenza associated with rs12252-C. 25314048

2014

dbSNP: rs8099917
rs8099917
0.010 GeneticVariation BEFREE Here we demonstrate that the presence of the IL-28B TG/GG genotype (rs8099917, minor-allele) was associated with increased seroconversion following influenza vaccination (OR 1.99 p = 0.038). 25503988

2014

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE Our meta-analysis suggests that IFITM3 rs12252 T>C polymorphism is significantly associated with increased risk of severe influenza but not with the chance of initial virus infection. 25778715

2015

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE The single-nucleotide polymorphism rs12252-C, which is rare in Caucasian populations, but much more common in the Han Chinese population, has been found in much higher homozygous frequency in patients with severe acute influenza. 25784441

2015

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE Our meta-analysis suggests a significant association between a minor IFITM3 allele (SNP rs12252-C) with severe influenza</span> susceptibility, but not in mild influenza subjects, in both UK Caucasians and Han Chinese population. 25942469

2015

dbSNP: rs1048479
rs1048479
0.010 GeneticVariation BEFREE In a second phase of the study, the rs113350588 and rs1048479 polymorphisms identified in this sample were genotyped in a sample of 356 subjects from the northern and northeastern regions of Brazil with a diagnosis of pandemic influenza. 26436774

2015

dbSNP: rs113350588
rs113350588
0.010 GeneticVariation BEFREE In a second phase of the study, the rs113350588 and rs1048479 polymorphisms identified in this sample were genotyped in a sample of 356 subjects from the northern and northeastern regions of Brazil with a diagnosis of pandemic influenza. 26436774

2015

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE Recent studies suggest an association between the Interferon Inducible Transmembrane 3 (IFITM3) rs12252 variant and the course of influenza infection. 27351739

2016

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE The only Spanish patient homozygous for rs12252-C had a neurological disorder (a known risk factor for severe IVI) and mild influenza. 27492307

2016

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE <b>Conclusion:</b><i>IFITM3</i> rs12252</span> CC genotype was associated with severity rather than susceptibility of IVI in Chinese population, and this strong effect was observed in all subtypes of seasonal influenza infection. 28713779

2017

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE Previous studies have reported associations of IFITM3 SNP rs12252 with severe influenza, but evidence of association and the mechanism by which risk is conferred remain controversial. 28714988

2017

dbSNP: rs12252
rs12252
0.100 GeneticVariation BEFREE rs12252 was not associated with susceptibility to influenza-related critical illness in children or with critical illness severity. 28531322

2017

dbSNP: rs2476601
rs2476601
0.010 GeneticVariation BEFREE There was no significant difference among healthy pregnant R620W carriers and non-carriers in H1N1 antibody seroconversion rates after influenza vaccination. 28723925

2017

dbSNP: rs34481144
rs34481144
0.010 GeneticVariation BEFREE We found evidence of a new association of rs34481144 with severe influenza in three influenza-infected cohorts characterized by different levels of influenza illness severity. 28714988

2017