Table 2.
Association Rank | Variant | Chromosome 17 Position† | Allele 1 | Allele 2 | Allele 1 Frequency‡ | Odds Ratio | P Value§ | R2 with rs11078928‖ | P Value, Adjusted¶ |
---|---|---|---|---|---|---|---|---|---|
1 | rs11078928 | 39,908,216 | C | T | 0.147 | 0.734 | 1.47 × 10−7 | 1.000 | NA |
2 | rs34120102 | 39,869,782 | A | G | 0.151 | 0.737 | 1.75 × 10−7 | 0.954 | 7.62 × 10−1 |
3 | rs12949100 | 39,900,936 | A | G | 0.147 | 0.737 | 1.99 × 10−7 | 1.000 | 3.75 × 10−1 |
4 | rs12232497 | 39,883,866 | C | T | 0.152 | 0.739 | 2.18 × 10−7 | 0.964 | 9.88 × 10−1 |
5 | rs35736272 | 39,876,427 | C | T | 0.152 | 0.741 | 2.58 × 10−7 | 0.964 | 8.44 × 10−1 |
6 | rs12939832 | 39,908,623 | A | G | 0.146 | 0.739 | 2.67 × 10−7 | 0.995 | 3.40 × 10−1 |
7 | rs2305480 | 39,905,943 | A | G | 0.154 | 0.747 | 4.04 × 10−7 | 0.950 | 9.68 × 10−1 |
8 | rs4795398 | 39,881,926 | T | C | 0.154 | 0.747 | 4.33 × 10−7 | 0.951 | 7.59 × 10−1 |
9 | rs35569035 | 39,879,371 | T | C | 0.154 | 0.748 | 5.40 × 10−7 | 0.951 | 6.31 × 10−1 |
10 | rs12936409 | 39,887,396 | T | C | 0.154 | 0.749 | 5.62 × 10−7 | 0.951 | 6.01 × 10−1 |
11 | rs10852935 | 39,875,421 | T | C | 0.156 | 0.751 | 6.59 × 10−7 | 0.938 | 6.64 × 10−1 |
12 | rs34189114 | 39,876,207 | T | C | 0.164 | 0.762 | 1.41 × 10−6 | 0.885 | 7.17 × 10−1 |
13 | rs34074973 | 39,879,513 | G | GAGA | 0.164 | 0.763 | 1.60 × 10−6 | 0.885 | 6.64 × 10−1 |
14 | rs11557466 | 39,868,373 | T | C | 0.164 | 0.763 | 1.64 × 10−6 | 0.882 | 6.66 × 10−1 |
15 | rs4795400 | 39,910,767 | T | C | 0.169 | 0.770 | 1.64 × 10−6 | 0.856 | 9.00 × 10−1 |
16 | rs11078925 | 39,868,955 | C | T | 0.164 | 0.763 | 1.65 × 10−6 | 0.885 | 6.56 × 10−1 |
17 | rs5820308 | 39,913,111 | TCAAAA | T | 0.163 | 0.771 | 2.29 × 10−6 | 0.868 | 9.56 × 10−1 |
18 | rs62067029 | 39,882,138 | T | A | 0.154 | 0.686 | 2.58 × 10−6 | 0.951 | 3.38 × 10−1 |
19 | rs17608925 | 39,926,578 | C | T | 0.060 | 0.666 | 6.76 × 10−6 | 0.340 | 6.37 × 10−2 |
20 | rs59716545 | 39,875,604 | G | T | 0.164 | 0.706 | 9.04 × 10−6 | 0.885 | 7.63 × 10−1 |
21 | rs36000226 | 39,907,676 | C | T | 0.187 | 0.794 | 1.14 × 10−5 | 0.752 | 9.18 × 10−1 |
22 | rs2305479 | 39,905,964 | T | C | 0.187 | 0.795 | 1.20 × 10−5 | 0.752 | 8.92 × 10−1 |
23 | rs883770 | 39,907,128 | T | C | 0.187 | 0.795 | 1.26 × 10−5 | 0.752 | 8.97 × 10−1 |
24 | rs8076131 | 39,924,659 | G | A | 0.187 | 0.797 | 1.33 × 10−5 | 0.737 | 9.44 × 10−1 |
25 | rs56750287 | 39,906,691 | C | A | 0.179 | 0.794 | 1.42 × 10−5 | 0.794 | 6.25 × 10−1 |
26 | rs62067034 | 39,907,485 | T | C | 0.187 | 0.797 | 1.44 × 10−5 | 0.752 | 8.44 × 10−1 |
27 | rs11651596 | 39,899,863 | C | T | 0.255 | 0.818 | 1.49 × 10−5 | 0.525 | 3.77 × 10−1 |
28 | rs907092 | 39,766,006 | A | G | 0.174 | 0.792 | 1.53 × 10−5 | 0.716 | 9.62 × 10−1 |
29 | rs4795399 | 39,905,186 | C | T | 0.154 | 0.709 | 1.68 × 10−5 | 0.950 | 4.87 × 10−1 |
Definition of abbreviation: NA = not applicable.
Associations meta-analyzed across GCPD-A (Study of the Genetic Causes of Complex Pediatric Disorders–Asthma), SAGE II (Study of African Americans, Asthma, Genes and Environment), and SAPPHIRE (Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race–Ethnicity) using fixed-effect model. Case patients were individuals with reported asthma onset at an age of <5 years as compared with healthy control subjects. Associations below the threshold of P < 2.86 × 10−5 are listed.
Positions based on Genome Reference Consortium Human Build 38.
Allele frequencies are based on results from the participants without asthma in SAPPHIRE cohort.
Genotypes were analyzed using an additive model for the number of copies of allele 1 (coded as 0, 1, or 2); models were adjusted for patient sex and the first three principal components for population structure.
Linkage disequilibrium between given variant and rs11078928. Values of 1 imply perfect correlation between markers.
P value for the genotype association with asthma status after adjusting for rs11078928 genotype.