Nomenclature | rs | Nucleotide changes | Effect | n | Genotype frequencies, % | Allele frequencies, % | |||
---|---|---|---|---|---|---|---|---|---|
wt | ht | vt | p | q | |||||
CYP2C8*2 | rs11572103 | T805A | I269F | 383 | 99.22 | 0.78 | 0.00 | 99.61 | 0.39 |
CYP2C8*3 | rs11572080+ rs10509681 | G416A+ A1196G | R139K + K399R | 390 | 83.85 | 15.64 | 0.51 | 91.67 | 8.33 |
CYP2C9*2 | rs1799853 | C430T | R144C | 391 | 79.54 | 20.20 | 0.26 | 89.64 | 10.36 |
CYP2C9*3 | rs1057910 | A1075C | I359L | 394 | 81.22 | 17.77 | 1.02 | 90.10 | 9.90 |
CYP2C19*2 | rs4244285 | G681A | Splicing defect | 393 | 58.52 | 39.19 | 2.29 | 78.12 | 21.88 |
CYP2C19*3 | rs4986893 | G636A | W212X | 388 | 97.94 | 2.06 | 0.00 | 98.97 | 1.03 |
CYP3A4*1B | rs2740574 | A-392 G | 5'NTO change | 389 | 94.86 | 5.14 | 0.00 | 97.43 | 2.57 |
CYP3A4*2 | rs55785340 | T664C | S222P | 391 | 100.00 | 0.00 | 0.00 | 100.00 | 0.00 |
CYP3A5*3 | rs776746 | A6986G | R487C | 392 | 0.26 | 11.99 | 87.76 | 6.25 | 93.75 |
CYP2B6*5 | rs3211371 | C1459T | Splicing defect | 390 | 85.64 | 12.56 | 1.79 | 91.92 | 8.08 |