Gene-drug interactions (data source: DGIdb)
Gene Name Entrez ID Drug Name Chembl ID Interaction Types Sources publications
PCSK9 255738 RG-7652 CHEMBL2109539 inhibitor ChemblInteractions
PCSK9 255738 BOCOCIZUMAB CHEMBL3137349 inhibitor GuideToPharmacologyInteractions, ChemblInteractions
PCSK9 255738 EVOLOCUMAB CHEMBL2364655 inhibitor GuideToPharmacologyInteractions, ChemblInteractions
PCSK9 255738 Alirocumab CHEMBL2109540 inhibitor TdgClinicalTrial, GuideToPharmacologyInteractions, ChemblInteractions, DrugBank 26455563

Variant-drug associations (data source: PharmGKB)
Gene Name Variant Alleles Chemical Phenotype Category Significance Notes Sentence Publications Annotation ID
PCSK9 rs7552841 CT + TT atorvastatin efficacy no No significant difference in the % change in total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) or triglycerides (TG) were seen between the two genotype groups. Additionally, no significant differences in the basal levels or post-treatment levels were seen. 10 mg/day atorvastatin for 4 weeks. Genotypes CT + TT is not associated with response to atorvastatin in people with Hypercholesterolemia as compared to genotype CC. 26408409 1447674967
PCSK9 rs11591147 T hmg coa reductase inhibitors efficacy yes There was a 55.6% greater reduction in low-density lipoprotein cholesterol (LDL-C) in carriers of the T alleles as compared to those with the GG genotype. Note that carriers of the T allele were also associated with significantly decreased LDL-C levels at baseline (p=0.00022), though the result for response to statins was adjusted for this association. A p-value <0.0045 was considered statistically significant. The authors do not specify the composition of T allele carriers (i.e. heterozygotes, homozygotes, or both). Allele T is associated with increased response to hmg coa reductase inhibitors in people with Hypercholesterolemia as compared to genotype GG. 26902539 1447947045