rs2306283, SLCO1B1

N. diseases: 16
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
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
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
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
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
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