Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1061170
rs1061170
CFH
0.010 GeneticVariation BEFREE Of particular interest is association of CFS with two missense variants in genes of complement activation, rs4151667 (L9H) in CFB and rs1061170 (Y402H) in CFH. 26116897

2015

dbSNP: rs11214105
rs11214105
0.010 GeneticVariation BEFREE A 5' UTR polymorphism (rs11214105) in IL18 also associated with physical fatigue, body pain and score for CFS case defining symptoms. 26116897

2015

dbSNP: rs25531
rs25531
0.010 GeneticVariation BEFREE Maintenance of Chronic Fatigue Syndrome (CFS) in Young CFS Patients Is Associated with the 5-HTTLPR and SNP rs25531 A > G Genotype. 26473596

2015

dbSNP: rs4151667
rs4151667
0.010 GeneticVariation BEFREE Of particular interest is association of CFS with two missense variants in genes of complement activation, rs4151667 (L9H) in CFB and rs1061170 (Y402H) in CFH. 26116897

2015

dbSNP: rs4680
rs4680
0.010 GeneticVariation BEFREE Our results indicate a relationship of COMT polymorphism rs4680 with immune dysregulation in CFS providing a potential link for the association between stress and infection susceptibility in CFS. 26272340

2015

dbSNP: rs2247215
rs2247215
0.010 GeneticVariation BEFREE Subjects with the G allele of rs2247215 (GRIK2) were more likely to have CFS (p=0.0005), and CFS subjects showed decreased GRIK2 expression (10-fold; p=0.015). 21912186

2011

dbSNP: rs356653
rs356653
0.010 GeneticVariation BEFREE Subjects with the T allele of rs356653 (NPAS2) were more likely to have CFS (p=0.0007), and NPAS2 expression was increased (10-fold; p=0.027) in those with CFS. 21912186

2011

dbSNP: rs6311
rs6311
0.010 GeneticVariation BEFREE HTR2A was up-regulated in CFS through allele-specific expression modulated by transcription factors at critical sites in its promoter: an E47 binding site at position -1,438, (created by the A-allele of rs6311 polymorphism), a glucocorticoid receptor (GR) binding site encompassing a CpG at position -1,420, and Sp1 binding at CpG methylation site -1,224. 20941551

2011

dbSNP: rs821616
rs821616
0.010 GeneticVariation BEFREE Despite the variety of patients with CFS, DISC1 Ser704Cys has an association with CFS, which may also suggest that DISC1 plays a central role in the induction of various psychiatric diseases. 20227423

2010

dbSNP: rs1205738080
rs1205738080
0.010 GeneticVariation BEFREE Of the polymorphisms examined, three markers (-1438G/A, C102T, and rs1923884) all located in the 5-HT receptor subtype HTR2A were associated with CFS when compared to NF controls. 18079067

2008

dbSNP: rs1923884
rs1923884
0.010 GeneticVariation BEFREE Of the polymorphisms examined, three markers (-1438G/A, C102T, and rs1923884) all located in the 5-HT receptor subtype HTR2A were associated with CFS when compared to NF controls. 18079067

2008

dbSNP: rs369729113
rs369729113
0.010 GeneticVariation BEFREE Of the polymorphisms examined, three markers (-1438G/A, C102T, and rs1923884) all located in the 5-HT receptor subtype HTR2A were associated with CFS when compared to NF controls. 18079067

2008

dbSNP: rs6313
rs6313
0.010 GeneticVariation BEFREE Of the polymorphisms examined, three markers (-1438G/A, C102T, and rs1923884) all located in the 5-HT receptor subtype HTR2A were associated with CFS when compared to NF controls. 18079067

2008

dbSNP: rs763780
rs763780
0.010 GeneticVariation BEFREE We investigated the association between CFS and the frequency of rs763780, a C/T genetic polymorphism leading to His161Arg substitution in the IL-17F protein. 18774769

2008