Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518925
rs1057518925
COL6A2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057523354
rs1057523354
COL4A1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121918459
rs121918459
PTPN11
G 0.700 CausalMutation CLINVAR

dbSNP: rs1331463984
rs1331463984
TRAF7
A 0.700 CausalMutation CLINVAR

dbSNP: rs139194636
rs139194636
WARS2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553315329
rs1553315329
SPAST
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553621496
rs1553621496
UNC80
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554317002
rs1554317002
CDK13 ; LOC112267983
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555366607
rs1555366607
SPTB
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555889984
rs1555889984
RUNX1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1559931177
rs1559931177
QRICH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1560755661
rs1560755661
TBCK
A 0.700 CausalMutation CLINVAR

dbSNP: rs181109321
rs181109321
TTPA
T 0.700 GeneticVariation CLINVAR

dbSNP: rs551423795
rs551423795
MUSK
G 0.700 GeneticVariation CLINVAR

dbSNP: rs756877019
rs756877019
MUSK
C 0.700 GeneticVariation CLINVAR

dbSNP: rs757600616
rs757600616
WARS2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs864321670
rs864321670
ALDH18A1
T 0.700 CausalMutation CLINVAR

dbSNP: rs869312697
rs869312697
ARID1B
T 0.700 CausalMutation CLINVAR

dbSNP: rs3766246
rs3766246
FAAH
0.010 GeneticVariation BEFREE Genotypes at rs3766246 and rs2295633 were significantly associated with increased ratings of Arousal (p<0.05) and Fatigue (p<0.01) after the 10-mg dose. 19890266

2010
dbSNP: rs2295633
rs2295633
FAAH
0.010 GeneticVariation BEFREE Genotypes at rs3766246 and rs2295633 were significantly associated with increased ratings of Arousal (p<0.05) and Fatigue</span> (p<0.01) after the 10-mg dose. 19890266

2010
dbSNP: rs11214105
rs11214105
TEX12 ; LOC107987164
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: rs4719714
rs4719714
STEAP1B
0.010 GeneticVariation BEFREE An evaluation was done on whether genetic variation in a prominent proinflammatory cytokine, interleukin-6 (IL-6 c.-6101A>T [rs4719714]), was associated with mean ratings of evening fatigue, morning fatigue, and sleep disturbance, as well as with the trajectories of these symptoms. 20570482

2010
dbSNP: rs3087243
rs3087243
CTLA4
0.010 GeneticVariation BEFREE Besides, patients carrying A allele of rs3087243 had significantly lower score of fatigue domain than those carrying G allele (2.5 ± 0.8 vs 3.9 ± 1.3, P < 0.001). 23432218

2013
dbSNP: rs36010656
rs36010656
SLCO1C1
0.010 GeneticVariation BEFREE Both the OATP1C1-intron3C > T and the OATP1C1-C3035T polymorphism, but not the OATP1C1-Pro143Thr polymorphism, were associated with symptoms of fatigue and depression. 18410547

2008
dbSNP: rs4680
rs4680
COMT ; MIR4761
0.010 GeneticVariation BEFREE Catechol-O-methyltransferase genotype (Val158met) modulates cancer-related fatigue and pain sensitivity in breast cancer survivors. 21898113

2012