rs17111503, PCSK9

N. diseases: 7
Disease: Infarction, Lacunar ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Infarction, Lacunar
CUI: C0333559
Disease: Infarction, Lacunar
0.010 GeneticVariation BEFREE Our findings suggest that the <i>PCSK9</i> rs1711</span>1503 (G > A) polymorphism is associated with susceptibility to lacunar infarction in the Han population but not in the Uygur population. 28966647 2017