Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12252
rs12252
0.040 GeneticVariation BEFREE Moreover, the risk of <i>IFITM3</i> rs12252-C variant for severe IVI was specific for both influenza A and influenza B. 28713779

2017

dbSNP: rs12252
rs12252
0.040 GeneticVariation BEFREE Several studies suggest that the CC genotype at the single nucleotide polymorphism (SNP) rs12252 of IFITM3 confers a genetic predisposition to pandemic influenza A in Europeans and Han Chinese, although one study in a British cohort failed to show an association. 28813716

2017

dbSNP: rs12252
rs12252
0.040 GeneticVariation BEFREE The IFITM3 rs12252 variant was associated with respiratory infection hospitalization but not specifically in patients infected with Influenza A(H1N1)pdm09. 27351739

2016

dbSNP: rs12252
rs12252
0.040 GeneticVariation BEFREE IFITM3 polymorphism rs12252-C restricts influenza A viruses. 25314048

2014

dbSNP: rs121434431
rs121434431
0.010 GeneticVariation BEFREE We report three unrelated children with influenza A virus (IAV) infection manifesting as acute respiratory distress syndrome (IAV-ARDS), heterozygous for rare <i>TLR3</i> variants (P554S in two patients and P680L in the third) causing autosomal dominant (AD) TLR3 deficiency. 31217193

2019

dbSNP: rs1801274
rs1801274
0.010 GeneticVariation BEFREE Host genomic DNA was isolated from pharyngeal samples of 110 patients from northern Greece with severe (n = 59) or mild (n = 51) influenza A(H1N1)pdm09 disease, at baseline, and the genotype of CD55 rs2564978, C1QBP rs3786054 and FCGR2A rs1801274 SNPs was investigated. 30306260

2019

dbSNP: rs2275913
rs2275913
0.010 GeneticVariation BEFREE Also, the absence of A allele in IL-17 rs2275913 SNP increased the risk of influenza A (H1N1) infection (P = 0.008). 31196204

2019

dbSNP: rs2564978
rs2564978
0.010 GeneticVariation BEFREE Host genomic DNA was isolated from pharyngeal samples of 110 patients from northern Greece with severe (n = 59) or mild (n = 51) influenza A(H1N1)pdm09 disease, at baseline, and the genotype of CD55 rs2564978, C1QBP rs3786054 and FCGR2A rs1801274 SNPs was investigated. 30306260

2019

dbSNP: rs333
rs333
0.010 GeneticVariation BEFREE Human CCR5Δ32 (rs333) polymorphism has no influence on severity and mortality of influenza A(H1N1)pdm09 infection in Brazilian patients from the post pandemic period. 30389547

2019

dbSNP: rs3786054
rs3786054
0.010 GeneticVariation BEFREE Host genomic DNA was isolated from pharyngeal samples of 110 patients from northern Greece with severe (n = 59) or mild (n = 51) influenza A(H1N1)pdm09 disease, at baseline, and the genotype of CD55 rs2564978, C1QBP rs3786054 and FCGR2A rs1801274 SNPs was investigated. 30306260

2019

dbSNP: rs774024297
rs774024297
0.010 GeneticVariation BEFREE Importantly, Mal-D96N genetic variation confers a physiological protective phenotype to in vivo models of LPS-, <i>Escherichia coli</i>-, and influenza A virus-induced hyperinflammatory disease in a gene dosage-dependent manner. 30787108

2019

dbSNP: rs1129293
rs1129293
0.010 GeneticVariation BEFREE In humans, we tested the genetic association of disease severity in influenza A/H1N1pdm09-infected patients with three potentially functional <i>PIK3CG</i> single-nucleotide polymorphisms (SNPs), rs1129293, rs17847825, and rs2230460. 29867955

2018

dbSNP: rs17847825
rs17847825
0.010 GeneticVariation BEFREE We observed that SNPs rs17847825 and rs2230460 (A and T alleles, respectively) were significantly associated with protection from severe disease using the recessive model in patients infected with influenza A</span>(H1N1)pdm09. 29867955

2018

dbSNP: rs1800896
rs1800896
0.010 GeneticVariation BEFREE IL10 rs1800896 "C/A" genotype was significantly associated with fatality in influenza A/H1N1pdm09 infections. 30475169

2018

dbSNP: rs2230460
rs2230460
0.010 GeneticVariation BEFREE We observed that SNPs rs17847825 and rs2230460 (A and T alleles, respectively) were significantly associated with protection from severe disease using the recessive model in patients infected with influenza A(H1N1)pdm09. 29867955

2018

dbSNP: rs7629263
rs7629263
0.010 GeneticVariation BEFREE The E119D neuraminidase mutation identified in a multidrug-resistant influenza A(H1N1)pdm09 isolate severely alters viral fitness in vitro and in animal models. 27185624

2016

dbSNP: rs16944
rs16944
0.010 GeneticVariation BEFREE The IL6 rs1818879 (GA) heterozygous genotype was associated with severe influenza A (H1N1) virus infection (odds ratio [OR] = 5.94, 95% confidence interval [CI] 3.05-11.56), and two IL1B SNPs, rs16944 AG and rs3136558 TC, were associated with a decreased risk of infection (OR = 0.52 and OR = 0.51, respectively). 26657940

2015

dbSNP: rs1818879
rs1818879
0.010 GeneticVariation BEFREE The IL6 rs1818879 (GA) heterozygous genotype was associated with severe influenza A (H1N1) virus infection (odds ratio [OR] = 5.94, 95% confidence interval [CI] 3.05-11.56), and two IL1B SNPs, rs16944 AG and rs3136558 TC, were associated with a decreased risk of infection (OR = 0.52 and OR = 0.51, respectively). 26657940

2015

dbSNP: rs28454025
rs28454025
0.010 GeneticVariation BEFREE Hence, and assuming that rs28454025 is likely to be a false positive, no major genetic factor was detected that could explain poor influenza A course. 26379185

2015

dbSNP: rs3136558
rs3136558
0.010 GeneticVariation BEFREE Genetic susceptibility was determined (pA/H1N1 vs. AHC): the LTA rs909253 TC heterozygous genotype conferred greater risk (OR = 1.9), and a similar association was observed with the IL1B rs3136558 CC genotype (OR = 1.89). 26657940

2015

dbSNP: rs909253
rs909253
0.010 GeneticVariation BEFREE Genetic susceptibility was determined (pA/H1N1 vs. AHC): the LTA rs909253 TC heterozygous genotype conferred greater risk (OR = 1.9), and a similar association was observed with the IL1B rs3136558 CC genotype (OR = 1.89). 26657940

2015

dbSNP: rs524991
rs524991
0.010 GeneticVariation BEFREE A common genetic variant (rs524991, P=6.15E-08) as well as past influenza A (P=0.024) or B (P=0.006) infection were identified as predisposing factors for NMDAR-AB seropositivity. 23999527

2014