rs138207257, HOGA1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Renal Insufficiency
CUI: C1565489
Disease: Renal Insufficiency
0.010 GeneticVariation BEFREE The p.Pro190Leu mutation was reported with impaired renal function at follow-up; however, the p.Gly287Val was presented with normal renal function. 27561601 2017