Disease: Gilbert Disease (disorder) ×
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: rs35350960
rs35350960 		0.925 0.080 2 233760973 missense variant C/A;T snv 1.5E-03; 4.4E-05
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.730 1.000 3 2001 2007