Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4818
rs4818
COMT ; MIR4761
0.020 GeneticVariation BEFREE The rs4818 GG genotype was more strongly associated with FM compared to the CC genotype (OR = 1.680, 95% CI: 1.057, 2.672, p = 0.027). 26849490

2016
dbSNP: rs4818
rs4818
COMT ; MIR4761
0.020 GeneticVariation BEFREE For the SNP rs4818, the frequency of mutant genotype CC was 73.21 and 39.09% for patients with FS and </span>controls, respectively. 21120493

2012