Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2306283
rs2306283
0.030 GeneticVariation BEFREE Our conclusion suggests that the interaction between the SLCO1B1 388A>G and 521T>C polymorphisms could be an important genetic determinant of hepatic function and the therapeutic efficiency of simvastatin in Chinese patients with hyperlipidemia. 30336686

2018

dbSNP: rs2306283
rs2306283
0.030 GeneticVariation BEFREE The SLCO1B1 521T > C and 388A > G variants were found to be relatively common in Chinese patients with essential hyperlipidemia. 23263738

2013

dbSNP: rs2306283
rs2306283
0.030 GeneticVariation BEFREE The present study found that the allele frequencies of SLCO1B1 388A>G and 521T>C in Chinese patients with essential hyperlipidemia are comparable to those in healthy Chinese population. 20140004

2010