COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Breast Carcinoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs764392202
rs764392202
Entrez Id: 1312;100616414
Gene Symbol: COMT;MIR4761
COMT;MIR4761
CUI: C0678222
Disease:
Breast Carcinoma 		0.010 GeneticVariation BEFREE In summary, the BRCA1 Cys39Gly</span> and CYP17A1 -34T>C genetic variations were associated with breast cancer risk. 29510000 2018