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. Author manuscript; available in PMC: 2017 Jan 1.
Published in final edited form as: Clin Exp Allergy. 2016 Jan;46(1):112–124. doi: 10.1111/cea.12642

Figure 3.

Figure 3

SNP associations with RhinoGen, COPSAC, and COAST phenotypes. STAT4 rs4853546 genotype association with asthma (P=0.031) in RhinoGen (A) and asthma exacerbations (P=0.024) in COPSAC (B). JAK2 rs3780375 genotype association with mean number of illnesses (P=0.019) in RhinoGen (C) and wheezing illnesses (P=0.012) in COAST (D). MX1 rs469390 genotype association with viral asthma symptom burden (P=0.031) in RhinoGen (E) and asthma exacerbations (P=8.8x10−4) in COPSAC (F). DDX58 rs10813831 genotype association with loss of asthma control (P=0.0055) in RhinoGen (G) and asthma at age 6 years (P=0.035) in COAST (H). Error bars show standard error of means or proportions. Total number of individuals is indicated beneath each genotype class.