COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Neural Tube Defects ×
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: C0027794
Disease:
Neural Tube Defects 		0.010 GeneticVariation BEFREE No interaction was found between COMT rs4680 AA/AG and MTHFR CT/TT genotypes for total NTDs or any subtype of NTD. 24990354 2015