COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Major Depressive Disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs737865
rs737865
Entrez Id: 1312;10587
Gene Symbol: COMT;TXNRD2
COMT;TXNRD2
CUI: C1269683
Disease:
Major Depressive Disorder 		0.010 GeneticVariation BEFREE Additionally, we observed an association between rs737865 alleles and early onset MD (p=0.04). 21600957 2011