rs1489694587, DMD

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Paget Disease
CUI: C1368019
Disease: Paget Disease
0.010 GeneticVariation BEFREE Our results suggest that the ER alpha PvuII/XbaI and CaSR A986S polymorphisms may contribute to genetic susceptibility to Paget's disease. 14997007 2004
Osteitis Deformans
CUI: C0029401
Disease: Osteitis Deformans
0.010 GeneticVariation BEFREE Our results suggest that the ER alpha PvuII/XbaI and CaSR A986S polymorphisms may contribute to genetic susceptibility to Paget's disease. 14997007 2004
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
0.010 GeneticVariation BEFREE The A986S CaR polymorphism is the most common in Italian PHPT patients and the allotype AS does not appear to play a relevant role in the pathogenesis of PHPT and its severity. 12150336 2003