DRD2, dopamine receptor D2, 1813

N. diseases: 437; N. variants: 42
Disease: Alagille Syndrome ×
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: rs6276
rs6276 		0.807 0.320 11 113410675 3 prime UTR variant C/T snv 0.54
CUI: C0085280
Disease: Alagille Syndrome
Alagille Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases 0.010 1.000 1 2010 2010