HNF4A, hepatocyte nuclear factor 4 alpha, 3172

N. diseases: 340; N. variants: 74
Disease: Serum triglycerides increased ×
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: rs1568731279
rs1568731279 		0.925 0.160 20 44414506 splice acceptor variant G/A snv
CUI: C0813230
Disease: Serum triglycerides increased
Serum triglycerides increased 		Nutritional and Metabolic Diseases 0.700 0