MT2A, metallothionein 2A, 4502

N. diseases: 117; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder
0.310 GeneticVariation disease BEFREE The significance of the MT(2) receptor gene and the risk of rDD are suggested. 21353709 2011
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder
0.310 Biomarker disease PSYGENET The significance of the MT(2) receptor gene and the risk of rDD are suggested. 21353709 2011