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Table 3 Results from association studies in all familial CRC (cases A) and sub-cohort of families with colorectal-, gastric- and prostate cancer (cases B)

From: A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives

Locus

SNP

Gene

Type

Ref

Alt

Cases A

Controls

OR

p

Cases B

OR

p

3q29

rs181290971

PCYT1A

3' UTR

G

A

808

1510

0.83

0.66

283

1.06

0.90

3q29

rs41299376

TFRC

3' UTR

T

A

819

1526

1.25

0.26

293

1.61

0.07

3q29

rs754397679

PCYT1A

missense

C

T

785

1447

0

0

284

0

0

4q26

rs141180741

SEC24D

missense

G

A

818

1514

0.83

0.66

293

1.08

0.82

4q26

rs184578242

METTL14

3' UTR

A

G

819

1527

0.51

0.12

293

0.62

0.43

4q26

rs35392900

SEC24D

missense

G

C

813

1505

0.87

0.64

292

1.14

0.72

4q35.1

rs73872825

ENPP6

intron

A

G

811

1473

1.14

0.50

292

1.06

0.85

13q13

rs118015060

SMAD9

3' UTR

A

G

819

1527

1.02

0.92

293

1.39

0.27

13q33.3

rs56393169

MYO16

3' UTR

T

C

819

1526

1.08

0.51

293

1.24

0.19

16q23.3

rs72807847

CDH13

missense

A

G

819

1527

1.40

0.37

293

1.63

0.33

  1. Markers supporting the hypothesis in bold
  2. SNP single nucleotide polymorphism, OR odds ratio, p = p-value