TPH2, tryptophan hydroxylase 2, 121278

N. diseases: 137; N. variants: 37
Disease: Severe depression ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0588008
Disease: Severe depression
Severe depression 		0.010 GeneticVariation disease BEFREE A variant of TPH2 that encodes the R441H substitution (TPH2-R441H) was identified in individuals with severe depression. 31071306 2019