Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12584920
rs12584920
Entrez Id: 3356
Gene Symbol: HTR2A
HTR2A
CUI: C3178789
Disease:
Widespread Chronic Pain
0.010 GeneticVariation BEFREE There was an increased likelihood of having CWP in subjects with 1 or 2 copies of the T allele of rs12584920 (odds ratio [OR] 1.64, 95% confidence interval [95% CI] 1.01-2.60 [P = 0.03] in the discovery cohort, and OR 1.46, 95% CI 1.07-2.00 [P = 0.018] in the validation cohort). 21305503 2011