DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Hypertensive disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1201177282
rs1201177282
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE In AI patients, the presence of the haplotype 2 of BclI and N363S is associated with the presence of AH, Fx and with the combination of Fx and AH. 20584071 2010