DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Hyperparathyroidism, Primary ×
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: 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