Table 3.
Variant | Classifications | Frequency |
---|---|---|
ABCB1 2677 G > T/A‡ | TT,TA and AA | 40 (32.8%) |
GT and GA | 53 (43.4%) | |
GG | 29 (23.8%) | |
ABCB1 3435 C>T‡ | TT | 17 (13.9%) |
TC | 54 (44.3%) | |
CC | 51 (41.8%) | |
ABCB1 2677 Allele§ | T/A | 133 (54.5%) |
G | 111 (45.5%) | |
ABCB1 3435 Allele§ | T | 88 (36.1%) |
C | 156 (63.9%) | |
Diplotype‡ | 2677G/3435C‐2677G/3435C | 37 (30.3%) |
2677T/A/3435T‐2677 T/A/3435T | 15 (12.3%) | |
2677†/3435†‐2677†/3435† | 70 (57.4%) |
Any combination of alleles that is not mutually exclusive with another diplotype consisting of the 2677 and 3435 SNPs.
Number represents number of patients (percentage).
Number represents number of alleles (percentage).