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. Author manuscript; available in PMC: 2013 Oct 1.
Published in final edited form as: Arthritis Rheum. 2012 Oct;64(10):3463–3471. doi: 10.1002/art.34496

Table 1.

SNPs associated with GPA, listed in order of P-value.

Chr SNP Disease(s)* Gene(s) A WGGER Toronto S Meta-analysis
OR (95% CI) P OR (95% CI) P OR (95% CI) P
2 rs3087243 RA,T1D CTLA4 A 0.80 (0.66–0.97) 0.03 0.78 (0.67–0.91) 0.001 I 0.79 (0.70–0.89) 9.83E-05
2 rs231735 RA CTLA4 G 0.84 (0.69–1.02) 0.08 0.81 (0.70–0.94) 0.005 G 0.82 (0.73–0.92) 0.001
1 rs2476601 CD,Ps,RA,SLE,T1D PTPN22 A 1.24 (0.92–1.69) 0.16 1.41 (1.12–1.79) 0.004 G 1.35 (1.12–1.62) 0.002
20 rs4810485 RA CD40 T 0.80 (0.64–1.01) 0.05 0.81 (0.68–0.96) 0.02 I 0.81 (0.70–0.92) 0.002
1 rs3766606 Celiac PARK7,DJ-1 T 0.79 (0.61–1.02) 0.07 0.80 (0.66–0.98) 0.03 I 0.80 (0.68–0.94) 0.005
16 rs4788084 T1D IL27 T 1.13 (0.94–1.37) 0.19 1.21 (1.04–1.41) 0.01 G 1.18 (1.05–1.33) 0.006
16 rs151181 CD IL27,others C 1.16 (0.96–1.40) 0.12 1.20 (1.02–1.41) 0.03 I 1.18 (1.05–1.34) 0.007
10 rs6584283 CD,UC NKX2-3 T 0.83 (0.69–1.00) 0.05 0.87 (0.75–1.01) 0.07 I 0.86 (0.76–0.96) 0.009
1 rs12727642 Celiac PARK7,TNFRSF9 A 0.81 (0.64–1.05) 0.11 0.81 (0.66–1.00) 0.05 G 0.81 (0.69–0.95) 0.01
10 rs11190140 CD,UC NKX2-3 T 0.85 (0.71–1.02) 0.08 0.87 (0.75–1.01) 0.07 G 0.86 (0.77–0.97) 0.01
13 rs9585056 T1D IDIN C 0.77 (0.62–0.96) 0.02 0.91 (0.76–1.09) 0.33 I 0.85 (0.74–0.98) 0.03
15 rs17574546 T1D RASGRP1 C 1.15 (0.92–1.44) 0.21 1.20 (0.99–1.44) 0.06 I 1.18 (1.02–1.36) 0.03
11 rs4963128 SLE PHRF1,KIAA1542 T 0.79 (0.64–0.97 0.02 0.92 (0.79–1.08) 0.32 G 0.87 (0.77–0.99) 0.03
6 rs11755527 T1D BACH2 G 1.17 (0.97–1.42) 0.10 1.12 (0.96–1.30) 0.16 I 1.14 (1.01–1.28) 0.03
9 rs10758669 CD JAK2 C 1.16 (0.95–1.41) 0.15 1.13 (0.97–1.32) 0.12 G 1.14 (1.01–1.29) 0.03
10 rs706778 RA IL2RA T 1.11 (0.92–1.33) 0.29 1.14 (0.98–1.33) 0.09 I 1.13 (1.00–1.27) 0.05

Abbreviations: Chr = chromosome; SNP = single nucleotide polymorphism designation; RA = rheumatoid arthritis; T1D = type 1 diabetes; CD = Crohn’s disease; Ps = psoriasis; SLE = systemic lupus erythematosus; UC = ulcerative colitis; A (in column heading) = allele used to calculate odds ratio; OR = odds ratio; CI = confidence interval; S = source of genotype in Toronto cohort (I = imputed, G = genotyped).

*

SNPs were included in genetic risk scores for the diseases listed.

Unadjusted P-values are shown. Only the top-ranked SNP had a P-value still <0.05 after adjustment for the false discovery rate (P*168/rank).