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. Author manuscript; available in PMC: 2018 Jan 1.
Published in final edited form as: Interv Cardiol Clin. 2017 Jan;6(1):141–149. doi: 10.1016/j.iccl.2016.08.010

Table 1. CYP2C19 phenotypes derived from CYP2C19 genotype.

Genotype Phenotype
*1/*1 Normal metabolizer (NM)
*2/*2, *2/*3, or other combination of two loss-of-function alleles Poor metabolizer (PM)
*1/*2, *1/*3, *2/*17 or other genotypes with a single loss-of-function allele Intermediate metabolizer (IM)
*1/*17 Rapid metabolizer (RM)
*17/*17 Ultra-rapid metabolizer (UM)

The IM phenotype assignment for genotypes with one loss-of-function and one gain-of-function allele (e.g. *2/*17) is based on evidence of increased platelet aggregation among clopidogrel treated patients with this genotype compared to the *1/*1 genotype, indicating that that the *17 allele is unable to completely compensate for reduced activity with the *2 allele.29 However, the data are not completely consistent, and thus the IM phenotype assignment is considered provisional.