Table 2 Evidence for signal of association at previously robustly replicated loci

From: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Collection

Gene

Chromosome

Reported SNP

WTCCC SNP

HapMap r2

TrendP value

Genotypic P value

CAD

APOE

19q13

*

rs4420638

-

1.7 × 10-01

1.7 × 10-01

CD

NOD2

16q12

rs2066844

rs17221417

0.23

9.4 × 10-12

4.0 × 10-11

CD

IL23R

1p31

rs11209026

rs11805303

0.01

6.5 × 10-13

5.9 × 10-12

RA

HLA-DRB1

6p21

*

rs615672

-

2.6 × 10-27

7.5 × 10-27

RA

PTPN22

1p13

rs2476601

rs6679677

0.75

4.9 × 10-26

5.6 × 10-25

T1D

HLA-DRB1

6p21

*

rs9270986

-

4.0 × 10-116

2.3 × 10-122

T1D

INS

11p15

rs689

-

-

-

T1D

CTLA4

2q33

rs3087243

rs3087243

1

2.5 × 10-05

1.8 × 10-05

T1D

PTPN22

1p13

rs2476601

rs6679677

0.75

1.2 × 10-26

5.4 × 10-26

T1D

IL2RA

10p15

rs706778

rs2104286

0.25

8.0 × 10-06

4.3 × 10-05

T1D

IFIH1

2q24

rs1990760

rs3788964

0.26

1.9 × 10-03

7.6 × 10-03

T2D

PPARG

3p25

rs1801282

rs1801282

1

1.3 × 10-03

5.4 × 10-03

T2D

KCNJ11

11p15

rs5219

rs5215

0.9

1.3 × 10-03

5.6 × 10-03

T2D

TCF7L2

10q25

rs7903146

rs4506565

0.92

5.7 × 10-13

5.1 × 10-12

  1. Where information on the strength of association at a particular SNP had been previously published and replicated we tabulated the P value of both the trend and genotype test at the same SNP (if in our study), or the best tag SNP (defined to be the SNP with highest r2 with the reported SNP, calculated in the CEU sample of the HapMap project). Positions are in NCBI build-35 coordinates. *Previous reports relate to haplotypes rather than single SNPs. Not well tagged by SNPs that pass the quality control, see main text.