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. Author manuscript; available in PMC: 2016 Jul 1.
Published in final edited form as: Pharmacogenet Genomics. 2015 Jul;25(7):343–353. doi: 10.1097/FPC.0000000000000143

Table 3.

Frequencies of predicted diplotypes known to affect warfarin dose in the CANHR and SCF datasets.

CANHR Diplotype Frequencies
VKORC1 diplotype CYP2C9 diplotype
*1/*1 *1/*2 *1/*3 *2/*2 *1/M1L *1/N218I *1/*29 M1L/M1L *3/M1L Total
Low dose homozygous (AT/AT) 153 1 6 0 25 20 12 2 3 222
Low dose heterozygous (AT/GC) 77 0 3 1 13 6 1 1 0 102
High dose homozygous (GC/GC) 17 1 2 0 4 1 0 1 0 26
Total 247 2 11 1 42 27 13 4 3 350
SCF Diplotype Frequencies
VKORC1 diplotype CYP2C9 diplotype
*1/*1 *1/*2 *1/*3 *2/*2 *1/M1L *1/N218I *2/N218I *2/*3 *3/*3 Total
Low dose homozygous (AT/AT) 101 10 5 0 4 3 0 1 0 124
Low dose heterozygous (AT/GC) 145 15 10 1 1 5 1 0 1 179
High dose homozygous (GC/GC) 41 7 5 0 1 1 0 1 0 56
Total 287 32 20 1 6 9 1 2 1 359

Diplotypes of VKORC1 and CYP2C9 were calculated from observed 1173 and -1639-containing high and low dose VKORC1 haplotypes, and CYP2C9 *1, *2, *3 and the M1L, N218I, and P279T genotypes, assuming no LD between CYP2C9 variants.