COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: manic symptom ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4680
rs4680
Entrez Id: 1312;100616414
Gene Symbol: COMT;MIR4761
COMT;MIR4761
CUI: C0746402
Disease:
manic symptom 		0.010 GeneticVariation BEFREE These results suggest that COMT striatal activity, but not rs4680 genotype, may serve as a biomarker for manic symptoms. 27458023 2017