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Table 3 Replication results for the already-described loci

From: A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12

SNP REF

LOCUS

REPORTED ALLELE

REPORTED MAF

ALLELIC OR (95% CI)

BEST PROXY AFFY 6.0

R2

OR (95% CI)

EPICOLON P value

rs6687758

1q41

G

0.2

1.09 (1.06-1.12)

rs6691195

1

1.10 (0.92-1.33)

0.291

rs6691170

1q41

T

0.34

1.06 (1.03-1.09)

rs11579490

0.902

1.00 (0.86-1.17)

0.974

rs10936599

3q26

T

0.24

0.93 (0.91-0.96)

rs7621631

1

0.99 (0.83-1.19)

0.970

rs16892766

8q23

C

0.07

1.32 (1.21-1.44)

rs2437844

0.925

1.13 (0.87-1.46)

0.360

rs6983267

8q24

T

0.48

0.83 (0.79-0.87)

rs6983267

-

0.87 (0.75-1.01)

0.065

rs10795668

10p14

A

0.33

0.91 (0.86-0.96)

rs706771

0.896

0.89 (0.76-1.04)

0.15

rs3802842

11q23

C

0.29

1.21 (1.15-1.27)

rs3802840

1

1.19 (1.01-1.40)

0.037

rs11169552

12q13

T

0.26

0.92 (0.90-0.95)

rs11169544

1

0.99 (0.83-1.18)

0.891

rs7136702

12q13

T

0.35

1.06 (1.03-1.09)

rs7136702

-

1.14 (0.98-1.33)

0.0806

rs4444235

14q22

C

0.46

1.12 (1.07-1.18)

rs11623717

0.838

1.01 (0.88-1.17)

0.859

rs1957636

14q22

A

0.39

1.08 (1.06-1.11)

rs4901475

0.932

1.16 (0.99-1.34)

0.153

rs16969681

15q13

T

0.09

1.18 (1.11-1.25)

rs16969344

1

1.21 (0.96-1.53)

0.103

rs11632715

15q13

A

0.46

1.12 (1.08-1.16)

rs12592288

0.524

1.04 (0.81-1.12)

0.589

rs9929218

16q22

A

0.29

0.88 (0.83-0.92)

rs7186084

1

0.94 (0.80-1.10)

0.439

rs4939827

18q21

C

0.47

0.85 (0.81-0.89)

rs7226855

1

0.82 (0.71-0.95)

8.204E-03

rs10411210

19q13

T

0.10

0.79 (0.72-0.86)

rs7252505

0.831

0.90 (0.72-1.13)

0.363

rs961253

20p12

A

0.36

1.13 (1.08-1.19)

rs5005940

1

1.11 (0.92-1.26)

0.349

rs4813802

20p12

G

0.36

1.09 (1.06-1.12)

rs4813802

-

1.07 (0.91-1.25)

0.433

rs4925386

20q13

T

0.32

0.93 (0.91-0.95)

rs4925386

-

0.96 (0.82-1.12)

0.61

  1. Association data for the 19 CRC risk variants (rs5934683 at Xp22.2 is not included). In bold two of the SNPs that showed direct evidences of association at a nominal p value<0.05.