We also found that the STYXL1-SRRM3 rs112463197 T allele had the highest OR (2.08, 95% CI = 1.19–3.64) in patients with Löfgren’s syndrome in the Czech cohort, and it had a higher OR in patients with CXR stages 0–II than in patients with stages III–IV in both the Japanese and Czech cohorts, although the trend was not significant. The gene discussed is STYXL1; the disease is Löfgren’s syndrome.