MAOB, monoamine oxidase B, 4129

N. diseases: 152; N. variants: 8
Disease: Hyperprolactinemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799836
rs1799836
Entrez Id: 4129
Gene Symbol: MAOB
MAOB
CUI: C0020514
Disease:
Hyperprolactinemia 		0.010 GeneticVariation BEFREE One statistically significant association between polymorphic variant rs1799836 of MAOB gene and HPRL in men was found in the total group. 30967134 2019