DRD2, dopamine receptor D2, 1813

N. diseases: 437; N. variants: 42
Disease: Myoclonic dystonia ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894220
rs104894220 		1.000 0.040 11 113416935 missense variant C/T snv 4.4E-05 6.3E-05
CUI: C1834570
Disease: Myoclonic dystonia
Myoclonic dystonia 		Nervous System Diseases 0.010 1.000 1 2000 2000