rs886043751, UMOD

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperuricemic Nephropathy, Familial Juvenile 1
CUI: C4551496
Disease: Hyperuricemic Nephropathy, Familial Juvenile 1
0.710 GeneticVariation BEFREE The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect. 17245395 2007
Hyperuricemic Nephropathy, Familial Juvenile 1
CUI: C4551496
Disease: Hyperuricemic Nephropathy, Familial Juvenile 1
0.710 GeneticVariation UNIPROT
Medullary Cystic Kidney Disease Type 2
CUI: C1859040
Disease: Medullary Cystic Kidney Disease Type 2
0.700 GeneticVariation UNIPROT