DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Paget Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1489694587
rs1489694587
Entrez Id: 1756
Gene Symbol: DMD
DMD
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