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. 2018 Oct 29;19:209. doi: 10.1186/s12931-018-0890-0

Table 4.

Associations with NHGRI-EBI asthma SNPs in COPDGene childhood asthma GWAS

NHW a Gene SNP Locus Effect Allele OR Rsq Freq (%) P-value b,d Adj P-value e
(385 cases, 4979 controls) IL1RL1 rs10197862 f 2q12.1 A 1.45 1.00 0.85 0.002 0.011
TSLP rs1837253g 5q22.1 T 1.07 0.75 0.414 1.000
RAD50 rs2244012f 5q31.1 G 1.05 0.78 0.579 1.000
IL13 rs1295686f 5q31.1 T 1.22 0.80 0.026 0.180
C11orf30-LRRC32 rs7130588g 11q13.5 G 1.23 0.64 0.008 0.054
GSDMB rs2305480f 17q21.1 G 1.22 0.44 0.009 0.060
GSDMA rs3894194f 17q21.1 A 1.18 0.94 0.47 0.029 0.201
AA a Gene SNP Locus Effect Allele OR Rsq Freq (%) P-value b,d Adj P-value e
(325 cases, 2342 controls) IL1RL1 rs10197862f 2q12.1 A 1.10 0.98 0.74 0.344 1.000
TSLP rs1837253g 5q22.1 C 1.11 0.28 0.283 1.000
RAD50 rs2244012f 5q31.1 G 1.05 0.57 0.603 1.000
IL13 rs1295686f 5q31.1 T 1.16 0.64 0.102 0.717
C11orf30-LRRC32 rs7130588g 11q13.5 G 1.23 0.80 0.035 0.247
GSDMB rs2305480f 17q21.1 G 1.03 0.13 0.817 1.000
GSDMA rs3894194f 17q21.1 G 1.02 0.88 0.69 0.846 1.000
Meta-analysis a Gene SNP Locus Effect Allele OR I 2 P-value c,d Adj P-value e
(710 cases, 7321 controls) IL1RL1 rs10197862 f 2q12.1 A 1.23 70 0.006 0.042
TSLP rs1837253g 5q22.1 C 1.01 45 0.910 1.000
RAD50 rs2244012f 5q31.1 G 1.05 0 0.447 1.000
IL13 rs1295686 f 5q31.1 T 1.19 0 0.006 0.043
C11orf30-LRRC32 rs7130588 g 11q13.5 G 1.23 0 0.001 0.005
GSDMB rs2305480f 17q21.1 G 1.17 27 0.018 0.125
GSDMA rs3894194f 17q21.1 A 1.10 57 0.113 0.794

Abbreviations: NHGRI-EBI National Human Genome Research Institute - European Bioinformatics Institute; SNP single nucleotide polymorphism; GWAS genome-wide association study; NHW Non-Hispanic Whites; AA African American; OR odds ratio of the effect allele; Rsq estimation of imputation quality; Freq frequency of effect allele; I2 heterogeneity index; a Each population was run as an independent analysis, and then combined in the meta-analysis: b Logistic regression based on case control status; c Fixed effect meta-analysis weighted by inverse variance. d Adjusted for sex, genetic ancestry. e Bonferroni correction for seven tests, SNPs with adjusted p < 0.05 in Bold. f SNP is in the reported gene, g SNP is near the reported gene