rs121917743, REN

N. diseases: 1
Disease: Hyperuricemic Nephropathy, Familial Juvenile 2 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperuricemic Nephropathy, Familial Juvenile 2
CUI: C2751310
Disease: Hyperuricemic Nephropathy, Familial Juvenile 2
0.800 GeneticVariation UNIPROT Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure. 19664745 2009
Hyperuricemic Nephropathy, Familial Juvenile 2
CUI: C2751310
Disease: Hyperuricemic Nephropathy, Familial Juvenile 2
0.800 GeneticVariation CLINVAR
Hyperuricemic Nephropathy, Familial Juvenile 2
CUI: C2751310
Disease: Hyperuricemic Nephropathy, Familial Juvenile 2
0.800 CausalMutation CLINVAR