NRG1, neuregulin 1, 3084

N. diseases: 304; N. variants: 65
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0233762
Disease: Hallucinations, Auditory
Hallucinations, Auditory
0.010 GeneticVariation phenotype BEFREE A significant linkage signal was observed on D8S1769, which is located 352 kb upstream of the 5' end of the first exon of NRG1 for two ("narrow" and "narrow with auditory hallucination (AH)") of the three adopted phenotype classes. 16526041 2006