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Table 2 Association testing of six T1D associated SNPs not previously investigated for association with RA in the current cohort

From: Overlapping genetic susceptibility variants between three autoimmune disorders: rheumatoid arthritis, type 1 diabetes and coeliac disease

SNP

CHR

position

Gene

MAF cases

MAF controls

P_HWE

case_11

case_12

case_22

control_11

control_12

control_22

P_trend

Allelic OR

(95% CI)

rs11755527

6

91014952

BACH2

0.46

0.46

0.91

729

(20.8)

1,790

(51.0)

990

(28.2)

669

(21.5)

1,551

(49.9)

891

(28.6)

0.86

0.99

(0.93 to 1.06)

rs689

11

2138800

INS

0.28

0.28

0.54

287

(8.2)

1,411

(40.1)

1,818

(51.7)

254

(8.2)

1,246

(40.0)

1,612

(51.8)

0.95

1.00

(0.93 to 1.08)

rs12708716

16

11087374

CLEC16A

0.36

0.36

0.63

507

(12.9)

1,791

(45.4)

1,643

(41.7)

453

(12.9)

1,596

(45.5)

1,455

(41.5)

0.88

1.00

(0.93 to 1.06)

rs3825932

15

77022501

CTSH

0.32

0.32

0.77

368

(10.5)

1,506

(43.1)

1,619

(46.3)

323

(10.4)

1,366

(44.1)

1,407

(45.4)

0.62

0.98

(0.91 to 1.06)

rs3788013

21

42714397

UBASH3A

0.45

0.43

0.86

705

(20.1)

1,752

(49.9)

1,052

(30.0)

590

(19.0)

1,522

(49.0)

996

(32.0)

0.07

1.07

(1.00 to 1.14)

rs229541

22

35921264

C1QTNF6

0.45

0.43

0.49

726

(20.6)

1,693

(48.1)

1,100

(31.3)

564

(18.1)

1,548

(49.6)

1,007

(32.3)

0.04

1.08

(1.00 to 1.15)

  1. 11 = homozygote for minor allele, 12 = heterozygote, 22 = homozygote for major allele; CHR, chromosome; MAF, minor allele frequency; P_HWE, P-value for Hardy Weinberg equilibrium test