Table 1: Frequency of alleles and diplotypes among patients tested in primary care whose DNA was fully genotyped
GeneAllele/diplotypeNo. (%) of patients (n = 185)95% confidence intervalPhenotype
SLCO1B1
rs4149056
T/T132 (71)64-77Normal function
T/C49 (26) 21-33Intermediate function
C/C4 (2) 0-4Low activity
G6PD
rs5030868
C/C185 (100)98-100Normal variant
C/T0 (0)0-2Variable activity
T/T0 (0)0-2Low activity
VKORC1
rs9923231
G/G38 (20)15-27Normal activity
G/A89 (48)41-55Intermediate activity
A/A58 (31)25-38Low activity
HLA-B*58:01*58:01 negative176 (95)91-97Normal
*58:01 positive7 (4)2-8Increased hypersensitivity
Undetermined2 (1)0-4Unknown
CYP2C19*1/*180 (43)36-50Extensive metabolizer
*1/*2,*2/*17,*1/*4,*1/*855 (30)24-37Intermediate metabolizer
*2/*2,*2/*3,*3/*38 (4)2-8Poor metabolizer
*1/*17,*17/*1742 (23)17-29Ultrarapid metabolizer
CYP2C9*1/*1,118 (64)57-70Extensive metabolizer
*1/*2,*1/*3,*2/*2,*2/*362 (34)27-41Intermediate metabolizer
*3/*35 (3)1-6Poor metabolizer
CYP2D6
Codeine CPIC guidelines†
*1/*1,*1,*2,*2/*2,*1/*10,(*10/*10)3N,(*2/*4)3N,*1/*17,*1/*3,*1/*4,*1/*5,*1/*41,*2/*10,*2/*4,*2/*5,*2/*9,*2/*41,*10/*10,*41/*41148 (80)74-85Extensive metabolizer
*3/*41,*3/*9,*4/*10,*4/*9,*4/*41,*5/*10,*5/*919 (10)7-15Intermediate metabolizer
*3/*4,*4/*14A,*4/*4,*4/*5,*4/*613 (7)4-12Poor metabolizer
(*1/*1)xN,(*1/*10)3N,(*1/*2)3N,(*2/*2)3N5 (3)1-6Ultrarapid metabolizer
CYP2D6
DPWG guidelines†
*1/*1,*1,*2,*1/*10,*1/*17,*1/*41,*2/*2,*2/*10,*2/*41,*2/*9,(*1/*10)3N94 (51)44-58Extensive metabolizer
(*2/*4)3N,*1/*3,*1/*4,*1/*5,*2/*4,*2/*3,*10/*10,(*10/*10)3N, *2/*5,*41/*41,*3/*41,*3/*9,*4/*9,*4/*10,*4/*41,*5/*10,*5/*974 (40)33-47Intermediate metabolizer
*3/*4,*4/*14A,*4/*4,*4/*5,*4/*613 (7)4-12Poor metabolizer
(*1/*1)xN,(*1/*2)3N,(*2/*2)3N4 (2)1-5Ultrarapid metabolizer

Note: CPIC = Clinical Pharmacogenetics Implementation Consortium, DPWG = Dutch Pharmacogenetics Working Group.

†Ambiguous genotypes DPWG CYP2D6 (*2/*4)3N and CPIC CYP2D6 (*1/*10)3N were assigned the "worst-case" phenotype.