rs6280, DRD3

N. diseases: 57
Disease: Abnormal involuntary movement ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Abnormal involuntary movement
CUI: C0392702
Disease: Abnormal involuntary movement
0.010 GeneticVariation BEFREE Interactive effects of cytochrome P 450 17alpha-hydroxylase with the dopamine D3 Ser9Gly polymorphism on abnormal involuntary movements were examined. 11839369 2002