Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs854560
rs854560
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.010 GeneticVariation BEFREE Our results suggest that the human serum paraoxonase polymorphisms, Q192R and L55M, are not associated with the risk of cerebral infarction in Chinese Han population. 16808888

2006