rs4633, COMT;MIR4761

N. diseases: 25
Disease: Fibromyalgia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
0.010 GeneticVariation BEFREE Although allele and genotype frequencies did not differ among groups, the rs4633 CT genotype was not associated with the presence of FM following adjustment for age and sex (OR = 0.745; 95% CI: 0.558, 0.995; p = 0.046). 26849490 2016