Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1732778
rs1732778
0.010 GeneticVariation BEFREE Statistically significant differences in genotype, allele, and haplotype frequencies for 3 OAS2 single nucleotide polymorphisms (rs1293762, rs15895, and rs1732778) and 2 OAS3 single nucleotide polymorphisms (rs2285932 and rs2072136) were detected between patients with central nervous system disease and both those with fever and/or meningitis and the control group. 21050126

2010

dbSNP: rs2808635
rs2808635
0.010 GeneticVariation BEFREE Specifically, correlations between SNPs and different levels of PDT-V efficacy have been detected by examining the gene variants influencing (i) thrombo-coagulative pathways, i.e. methylenetetrahydrofolate reductase (MTHFR) 677C>T (rs1801133), factor V (F5) 1691G>A (rs6025), prothrombin (F2) 20210G>A (rs1799963), and factor XIII-A (F13A1) 185G>T (rs5985); (ii) complement activation and/or inflammatory processes, i.e. complement factor H (CFH) 1277T>C (rs1061170), high-temperature requirement factor A1 (HTRA1) promoter -512G>A (rs11200638), and two variants of the C-reactive protein (CRP) gene (rs2808635 and rs876538); and (iii) production and bioavailability of vascular endothelial growth factor (VEGFA -2578C>A [rs699947] and rs2146323). 21913742

2011

dbSNP: rs876538
rs876538
0.010 GeneticVariation BEFREE Specifically, correlations between SNPs and different levels of PDT-V efficacy have been detected by examining the gene variants influencing (i) thrombo-coagulative pathways, i.e. methylenetetrahydrofolate reductase (MTHFR) 677C>T (rs1801133), factor V (F5) 1691G>A (rs6025), prothrombin (F2) 20210G>A (rs1799963), and factor XIII-A (F13A1) 185G>T (rs5985); (ii) complement activation and/or inflammatory processes, i.e. complement factor H (CFH) 1277T>C (rs1061170), high-temperature requirement factor A1 (HTRA1) promoter -512G>A (rs11200638), and two variants of the C-reactive protein (CRP) gene (rs2808635 and rs876538); and (iii) production and bioavailability of vascular endothelial growth factor (VEGFA -2578C>A [rs699947] and rs2146323). 21913742

2011

dbSNP: rs1045642
rs1045642
0.010 GeneticVariation BEFREE We found that patients carrying the CYP3A5*1/*3 genotype demonstrated more side effects of fever, pleural effusion, and febrile neutropenia than those with the CYP3A5*3/*3 genotype (p = 0.075, 0.077, and 0.030, respectively); moreover, patients with the ABCB1 2677G/G genotype also showed more side effects of fever and febrile neutropenia than those with other genotypes (p = 0.024 and 0.027), In regard to ABCB1 3435C>T, patients with ABCB1 3435C/C tended to suffer leucopenia (p = 0.057). 19332043

2009

dbSNP: rs11568658
rs11568658
0.010 GeneticVariation BEFREE The ABCC4 single nucleotide polymorphism rs11568658 was associated with misoprostol-induced fever. 26122863

2015

dbSNP: rs1554785242
rs1554785242
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554791280
rs1554791280
C 0.700 CausalMutation CLINVAR

dbSNP: rs11575933
rs11575933
0.010 GeneticVariation BEFREE This explains the higher susceptibility of the enzymatic activity of MDTCS-P475S to reaction environments such as denaturants and high temperature. 23621748

2013

dbSNP: rs1064797245
rs1064797245
0.010 GeneticVariation BEFREE A de novo p.Arg756Cys mutation in ATP1A3 causes a distinct phenotype with prolonged weakness and encephalopathy triggered by fever. 29066118

2018

dbSNP: rs72554640
rs72554640
T 0.700 CausalMutation CLINVAR

dbSNP: rs5743507
rs5743507
BPI
0.010 GeneticVariation BEFREE We evaluated the role of single nucleotide polymorphisms for five genes: bactericidal permeability increasing protein (BPI; rs5743507), lipopolysaccharide-binding protein (LBP; rs2232618), toll-like receptor 4 (TLR4; rs4986790), heat shock protein 70 (HSP 70; rs2227956), and interleukin 6 (IL-6; rs1800795) in 598 children aged 0 to 19 years that were admitted to a paediatric intensive care unit with fever, systemic inflammatory response syndrome, sepsis, severe sepsis, septic shock, or multiple organ dysfunction syndrome. 24383711

2014

dbSNP: rs2227288
rs2227288
0.010 GeneticVariation BEFREE However, the duration of fever, white blood cell (WBC) count, C-reactive protein (CRP), neutrophils, and lymphocytes and monocytes of virus-induced encephalitis patients with IL-4 rs2227288 and IL-10 rs1800872 all displayed significant differences (all P<0.05). 28935853

2017

dbSNP: rs2229291
rs2229291
0.020 GeneticVariation BEFREE The F352C variant results in energy crisis at high temperature and is suspected as a risk factor for acute encephalopathy. 23969168

2014

dbSNP: rs2229291
rs2229291
0.020 GeneticVariation BEFREE Positive association was found between rs2</span>229291 and patients with fever</span> at onset of seizure and degree of pathogenetic condition (P = 0.018 and P = 0.023), but not for rs1799821. 25361188

2014

dbSNP: rs1567608853
rs1567608853
C 0.700 CausalMutation CLINVAR

dbSNP: rs12939622
rs12939622
0.010 GeneticVariation BEFREE The AA genotype of rs12939622 (in the dominant model) and the AA genotype of rs4262994 (in the recessive model) caused increased susceptibility of the subjects to fever (P < .001 and P = .008, respectively). 31692082

2020

dbSNP: rs1187636039
rs1187636039
0.010 GeneticVariation BEFREE In the family assessed, the p.D294E mutation segregated in association with a particular sensitivity to cold exposure (especially arthralgias and myalgia), but not always with an inflammatory phenotype (e.g., urticarial rash or fever). 21360512

2011

dbSNP: rs755789256
rs755789256
0.010 GeneticVariation BEFREE Evaluation of a recombinant double mutant of staphylococcal enterotoxin B (SEB-H32Q/K173E) with enhanced antitumor activity effects and decreased pyrexia. 23405232

2013

dbSNP: rs3832879
rs3832879
0.010 GeneticVariation BEFREE Each patient underwent evaluation of serum FGF23 levels and FGF23 genotype: the frequency of the c.212-37insC (rs3832879) polymorphism in intron 1 was examined and compared with sex, age at disease onset, fever duration, laboratory data, and occurrence of CaA. 24168888

2013

dbSNP: rs7849782
rs7849782
0.010 GeneticVariation BEFREE According to univariate regression analysis, CAA formation in KD was significantly associated with fever duration (p < 0.0001), first Intravenous immunoglobulin (IVIG) used (days after day one of fever) (p < 0.0001), and the GRIN3A (rs7849782) genetic variant (p < 0.001). 24278430

2013

dbSNP: rs62641689
rs62641689
T 0.700 GeneticVariation CLINVAR

dbSNP: rs41550816
rs41550816
0.010 GeneticVariation BEFREE Evaluation of a recombinant double mutant of staphylococcal enterotoxin B (SEB-H32Q/K173E) with enhanced antitumor activity effects and decreased pyrexia. 23405232

2013

dbSNP: rs1057518886
rs1057518886
A 0.700 CausalMutation CLINVAR

dbSNP: rs2227956
rs2227956
0.010 GeneticVariation BEFREE We evaluated the role of single nucleotide polymorphisms for five genes: bactericidal permeability increasing protein (BPI; rs5743507), lipopolysaccharide-binding protein (LBP; rs2232618), toll-like receptor 4 (TLR4; rs4986790), heat shock protein 70 (HSP 70; rs2227956), and interleukin 6 (IL-6; rs1800795) in 598 children aged 0 to 19 years that were admitted to a paediatric intensive care unit with fever, systemic inflammatory response syndrome, sepsis, severe sepsis, septic shock, or multiple organ dysfunction syndrome. 24383711

2014

dbSNP: rs2069705
rs2069705
0.010 GeneticVariation BEFREE The association of IFN-γ rs2069705 with the risk of breast cancer was not significant among all participants, while the CT/TT genotypes were significantly related to an elevated risk of breast cancer [1.32 (1.03-1.70)] among the women with <1 fever per year and to a reduced risk of breast cancer [0.63 (0.40-0.99)] among women with ≥1 fever per year compared to the CC genotype. 22624006

2012