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. 2019 Aug 14;18:56–65. doi: 10.1016/j.omtn.2019.08.006

Table 2.

Genotype Frequencies of TYMS, GOLGA7, RYR3, and KIAA0423 Polymorphism in Cases and Controls

Model Genotype Control (%) Case (%) OR (95% CI) p Value
rs11337 HWE: p = 0.51

Co-dominant GG 779 (59.9) 384 (63.5) 1.00 (reference)
 Heterozygote GT 460 (35.4) 194 (32.0) 0.86 (0.70–1.05) 0.14
 Homozygote TT 61 (4.7) 27 (4.5) 0.90 (0.56–1.43) 0.65
Dominant GG 779 (59.9) 384 (63.5) 1.00 (reference) 0.14
GT+TT 521 (40.1) 221 (36.5) 0.86 (0.71–1.05)
Recessive GG+GT 1,239 (95.3) 578 (95.5) 1.00 (reference) 0.82
TT 61 (4.7) 27 (4.5) 0.95 (0.60–1.51)
Overdominant GG+TT 840 (64.6) 411 (68) 1.00 (reference) 0.16
GT 460 (35.4) 194 (32) 0.86 (0.7–1.06)
Allele
G 2,018 (77.6) 962 (79.5) 1.00 (reference) 0.19
T 582 (22.4) 248 (20.5) 0.89 (0.76–1.06)

rs1044129 HWE: p = 0.86

Co-dominant GG 259 (19.9) 106 (17.5) 1.00 (reference)
 Heterozygote GA 639 (49.2) 315 (52.1) 1.20 (0.93–1.57) 0.17
 Homozygote AA 402 (30.9) 184 (30.4) 1.12 (0.84–1.49) 0.44
Dominant GG 259 (19.9) 106 (17.5) 1.00 (reference) 0.22
GA+AA 1,041 (80.1) 499 (82.5) 1.17 (0.91–1.50)
Recessive GG+GA 898 (69.1) 421 (69.6) 1.00 (reference) 0.82
AA 402 (30.9) 184 (30.4) 0.98 (0.79–1.20)
Overdominant GG+AA 661 (50.8) 290 (47.9) 1.00 (reference) 0.24
GA 639 (49.2) 315 (52.1) 1.12 (0.93–1.36)
Allele
G 1,157 (44.5) 527 (43.6) 1.00 (reference) 0.58
A 1,443 (55.5) 683 (56.4) 1.04 (0.91–1.19)

rs1053667 HWE: p = 0.96

Co-dominant TT 969 (74.5) 465 (76.9) 1.00 (reference)
 Heterozygote CT 307 (23.6) 135 (22.3) 0.92 (0.73–1.15) 0.46
 Homozygote CC 24 (1.9) 5 (0.8) 0.43 (0.16–1.14) 0.08
Dominant TT 969 (74.5) 465 (76.9) 1.00 (reference) 0.27
CT+CC 331 (25.5) 140 (23.1) 0.88 (0.70–1.10)
Recessive TT+CT 1,276 (98.1) 600 (99.2) 1.00 (reference) 0.09
CC 24 (1.9) 5 (0.8) 0.44 (0.17–1.17)
Overdominant TT+CC 993 (76.4) 470 (77.7) 1.00 (reference) 0.53
CT 307 (23.6) 135 (22.3) 0.93 (0.74–1.17)
Allele
T 2,245 (86.3) 1,065 (88) 1.00 (reference) 0.16
C 355 (23.7) 145 (12) 0.86 (0.70–1.06)

rs1059394 HWE: p = 0.53

Co-dominant CC 131 (10.1) 80 (13.2) 1.00 (reference)
 Heterozygote CT 548 (42.1) 255 (42.2) 0.76 (0.56–1.04) 0.09
 Homozygote TT 621 (47.8) 270 (44.6) 0.71 (0.52–0.97) 0.03*
Dominant CC 131 (10.1) 80 (13.2) 1.00 (reference) 0.04*
CT+TT 1,169 (89.9) 525 (86.8) 0.74 (0.55–0.99)
Recessive CC+CT 679 (52.2) 335 (55.4) 1.00 (reference) 0.20
TT 621 (47.8) 270 (44.6) 0.88 (0.73–1.07)
Overdominant CC+TT 752 (51.9) 350 (57.8) 1.00 (reference) 1.00
CT 548 (42.1) 255 (42.2) 1.00 (0.82–1.22)
Allele
C 810 (31.2) 415 (34.5) 1.00 (reference) 0.05
T 1,790 (68.8) 795 (65.5) 0.87 (0.75–1.00)

rs2847153 HWE: p = 0.47

Co-dominant GG 534 (41.1) 223 (36.9) 1.00 (reference)
 Heterozygote GA 589 (45.3) 295 (48.9) 1.20 (0.97–1.48) 0.09
 Homozygote AA 177 (13.6) 86 (14.2) 1.16 (0.86–1.57) 0.32
Dominant GG 534 (41.1) 223 (36.9) 1.00 (reference) 0.09
GA+AA 766 (58.9) 381 (63.1) 1.19 (0.98–1.45)
Recessive GG+GA 1,123 (86.4) 518 (85.8) 1.00 (reference) 0.71
AA 177 (13.6) 86 (14.2) 1.05 (0.80–1.39)
Overdominant GG+AA 711 (44.7) 309 (51.2) 1.00 (reference) 0.15
GA 589 (45.3) 295 (48.8) 1.15 (0.95–1.39)
Allele G 1,657 (63.7) 741 (61.3) 1.00 (reference) 0.16
A 943 (36.3) 467 (38.7) 1.11 (0.96–1.28)

HWE, Hardy-Weinberg equilibrium; STR, subtotal resection; NTR, near-total resection; GTR, gross total resection; reference, OR = 1 is the reference compared with other genotypes. *p ≤ 0.05 indicates statistical significance.