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Table 2 Association between colorectal cancer risk and SNPs in the TAS2R16 region stratified by histology

From: Association between polymorphisms of TAS2R16 and susceptibility to colorectal cancer

SNP

Alleles (Major/minor)

Site

Case/Controla

MM vs Mmb

P value

MM vs mmb

P value

MM vs Mm+mmb

P value

MM + Mm vs mmb

P value

P trend

MM

Mm

mm

rs860170

A/G

All

785/653

846/681

245/184

1.04(0.9–1.22)

0.57

1.05(0.83–1.32)

0.69

1.05(0.9–1.21)

0.55

1.03(0.83–1.27)

0.82

0.37

Colon

447/653

487/681

141/184

1.03(0.87–1.23)

0.73

1.07(0.82–1.4)

0.52

1.04(0.88–1.23)

0.64

1.06(0.82–1.35)

0.67

0.37

Rectum

231/653

256/681

68/184

1.06(0.85–1.32)

0.61

1.02(0.74–1.43)

0.89

1.05(0.85–1.29)

0.64

0.99(0.73–1.36)

0.97

0.65

rs978739

A/G

All

830/693

777/678

182/156

0.97(0.83–1.13)

0.67

0.98(0.77–1.26)

0.89

0.97(0.84–1.12)

0.68

1(0.79–1.27)

0.99

0.65

Colon

487/693

422/678

97/156

0.9(0.75–1.07)

0.22

0.88(0.65–1.17)

0.37

0.89(0.75–1.05)

0.18

0.92(0.7–1.22)

0.58

0.18

Rectum

240/693

222/678

71/156

0.97(0.78–1.22)

0.82

1.36(0.97–1.9)

0.08

1.04(0.85–1.29)

0.68

1.37(1–1.89)

0.05

0.30

rs1357949

T/C

All

927/719

761/659

180/145

0.91(0.78–1.05)

0.20

0.95(0.74–1.23)

0.71

0.91(0.79–1.06)

0.22

1(0.78–1.27)

0.99

0.31

Colon

512/719

443/659

110/145

0.97(0.81–1.15)

0.72

1.09(0.82–1.46)

0.54

0.99(0.84–1.17)

0.92

1.11(0.84–1.46)

0.46

0.98

Rectum

292/719

211/659

50/145

0.78(0.63–0.97)

0.03

0.82(0.57–1.19)

0.30

0.79(0.64–0.97)

0.02

0.92(0.65–1.32)

0.66

0.06

rs1525489

T/C

All

1728/956

145/62

1/0

1.24(0.88–1.73)

0.22

-

-

1.22(0.88–1.70)

0.23

-

-

0.08

Colon

992/956

77/62

0/0

1.22(0.83–1.8)

0.30

-

-

1.22(0.83–1.8)

0.30

-

-

0.31

Rectum

505/956

53/62

1/0

1.59(1.03–2.43)

0.03

-

-

1.62(1.06–2.47)

0.03

-

-

0.007

rs6466849

G/A

All

1276/1024

524/452

62/52

0.97(0.83–1.14)

0.75

1.01(0.68–1.51)

0.95

0.98(0.84–1.14)

0.78

1.02(0.69–1.51)

0.92

0.40

Colon

748/1024

284/452

36/52

0.88(0.73–1.05)

0.16

0.97(0.61–1.53)

0.88

0.88(0.74–1.06)

0.18

1(0.64–1.58)

0.99

0.16

Rectum

376/1024

156/452

22/52

1(0.8–1.26)

0.97

1.25(0.73–2.15)

0.42

1.03(0.83–1.28)

0.79

1.25(0.73–2.13)

0.42

0.92

rs10268496

T/G

All

1200/951

596/510

100/70

0.92(0.79–1.07)

0.28

1.07(0.77–1.49)

0.70

0.94(0.81–1.08)

0.38

1.1(0.79–1.53)

0.57

0.81

Colon

678/951

342/510

62/70

0.94(0.79–1.12)

0.49

1.18(0.81–1.71)

0.39

0.97(0.82–1.15)

0.72

1.2(0.83–1.74)

0.33

0.79

Rectum

364/951

175/510

25/70

0.88(0.7–1.09)

0.24

0.86(0.53–1.41)

0.55

0.87(0.71–1.08)

0.21

0.9(0.55–1.46)

0.67

0.37

  1. aNumbers may not add up 100% to genotyping failure, covariate missing values or DNA depletion
  2. bMM vs Mm = Common homozygous carriers vs heterozygous; MM vs mm = Common homozygous vs rare homozygous; MM vs Mm + mm = Common homozygous vs heterozygous + rare homozygous (Dominant Model); MM + Mm vs mm = Common homozygous + heterozygous vs rare homozygous. Odds Ratio (95% confidence interval).All analysis are adjusted for age, gender and country of origin