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. 2017 Sep 4;50(3):823–834. doi: 10.4143/crt.2017.351

Table 2.

Frequencies of candidate gene loci subjected to subsequent validation

Gene rsID Genotype No. of patients (%) (n=185)
NUDT15 rs116855232 CC 142 (77.6)
CT 37 (20.2)
TT 4 (2.2)
APEX1 rs2307486 AA 155 (85.2)
AG 26 (14.3)
GG 1 (0.5)
ABCC4 rs2274407 GG 116 (62.7)
GT 62 (33.5)
TT 7 (3.8)
rs3765534 CC 156 (85.2)
CT 24 (13.1)
TT 3 (1.6)
rs11568658 CC 138 (75.0)
CA 41 (22.3)
AA 5 (2.7)
CYP4F2 rs2108622 CC 81 (44.0)
CT 77 (41.8)
TT 26 (14.1)
CYP1A1 rs4646422 CC 125 (68.7)
CT 51 (28.0)
TT 6 (3.3)
SLCO1B1 rs11045879 TT 74 (40.7)
TC 74 (40.7)
CC 34 (18.7)
rs4149056 TT 129 (70.5)
TC 51 (27.9)
CC 3 (1.6)
ITPA rs1127354 CC 131 (71.6)
CA 47 (25.7)
AA 5 (2.7)
rs7270101 AA 185 (100)
MTHFR rs1801131 TT 128 (69.2)
TG 54 (29.2)
GG 3 (1.6)
rs1801133 GG 61 (33.5)
GA 92 (50.5)
AA 29 (15.9)
rs1901133 GG 84 (45.9)
GA 87 (47.5)
AA 12 (6.6)
GRIA1 rs4958351 GG 178 (96.2)
AG 7 (3.8)
MOCOS rs594445 CC 92 (49.7)
AC 79 (42.7)
AA 14 (7.6)
PACSIN2 rs2413739 CC 155 (85.2)
CT 27 (14.8)
TPMT *1/*1 178 (96.2)
*1/*3C 7 (3.8)