MTNR1A, melatonin receptor 1A, 4543

N. diseases: 79; N. variants: 6
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia
0.010 GeneticVariation disease BEFREE Our results indicated a significant association between the haplotype ATG in the MTNR1A gene and non-TD. 20726823 2011