Gene: NR3C2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4306
Gene Symbol: NR3C2
NR3C2 		0.010 GeneticVariation disease BEFREE Mutants of the mineralocorticoid receptor cannot explain the frequent syndrome of pre-eclampsia. 19151144 2009