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. 2020 Feb 5;10:1862. doi: 10.1038/s41598-020-58741-w

Table 1.

Loci associated with a genome-wide significant threshold after the cross-disease meta-analysis of systemic sclerosis and Crohn’s disease.

Discovery Replication Discovery + Replication
SSc CD SSc-CD SSc CD SSc-CD
Region Gene SNP Test Allele P-value OR P-value OR P-value P-value OR P-value OR P-value
1p31.3 IL12RB2 rs6659932 A 2.47E-08 1.3 1.33E-04 0.79 1.54E-11 3.75E-03 1.13 3.44E-02 0.86 1.08E-11
5q31.1 IRF1 rs2548998 G 1.55E-03 1.27 3.09E-07 0.79 1.13E-08 2.00E-02 1.08 1.18E-03 0.88 2.18E-11
6p21.31 ZBTB9/BAK1 rs68191 C 8.15E-03 0.84 8.70E-06 1.39 8.33E-07 2.09E-04 0.82 1.56E-02 1.15 1.07E-10
17q21.2 STAT3 rs4796791 T 1.34E-03 1.13 1.52E-04 0.84 9.86E-07 3.85E-02 1.08 1.85E-02 0.90 2.52E-08

Results of the discovery and replication analysis for each individual disease and of the combined meta-analysis (discovery + replication) are shown.

SNP, single-nucleotide polymorphism; SSc, systemic sclerosis; CD, Crohn’s disease.