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: rs1800562
rs1800562
HFE ; LOC108783645
0.020 GeneticVariation BEFREE Male C282Y homozygotes with a serum ferritin level of 1000 mug per liter or more were more likely to report fatigue, use of arthritis medicine, and a history of liver disease than were men who had the wild-type gene. 18199861

2008
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: rs199682734
rs199682734
OPRM1
0.010 GeneticVariation BEFREE Other genetic associations were also observed in men but not women, such as greater 'feel effects' and anger, and reduced fatigue, in the dopamine D2 receptor (DRD2 C957T single nucleotide polymorphism) TT versus CT or CC genotypes. 18690117

2008
dbSNP: rs6277
rs6277
DRD2
0.010 GeneticVariation BEFREE Other genetic associations were also observed in men but not women, such as greater 'feel effects' and anger, and reduced fatigue, in the dopamine D2 receptor (DRD2 C957T single nucleotide polymorphism) TT versus CT or CC genotypes. 18690117

2008
dbSNP: rs267606640
rs267606640
AGL
0.010 GeneticVariation BEFREE Even heterozygous p.W1327X mutation carriers may present with mild non-progressive neuromuscular symptoms, such as exercise-induced myalgia and fatigue. 18924225

2008
dbSNP: rs121913507
rs121913507
KIT
0.010 GeneticVariation BEFREE Six other patients reported symptomatic improvement, including two with D816V KIT mutation-positive SM (one reported improvement in diarrhea and the other in fatigue).Other patients had no benefit.Imatinib was relatively well tolerated. 19193436

2009
dbSNP: rs121913682
rs121913682
KIT
0.010 GeneticVariation BEFREE Six other patients reported symptomatic improvement, including two with D816V KIT mutation-positive SM (one reported improvement in diarrhea and the other in fatigue).Other patients had no benefit.Imatinib was relatively well tolerated. 19193436

2009