rs6311, HTR2A

N. diseases: 41
Disease: Pain ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pain
CUI: C0030193
Disease: Pain
0.010 GeneticVariation BEFREE The polymorphic allele of SNP rs6311 was more frequent in patients with severe pain (p:0.03). 30973927 2019