COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Pain ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5993882
rs5993882
Entrez Id: 1312
Gene Symbol: COMT
COMT
CUI: C0030193
Disease:
Pain 		0.010 GeneticVariation BEFREE In subjects without depressive symptoms, rs5993882 was identified as the SNP most likely to be related to TMD pain. 22337325 2012