Skip to main content
. Author manuscript; available in PMC: 2014 Aug 1.
Published in final edited form as: Pharmacogenomics J. 2013 Mar 19;14(1):41–47. doi: 10.1038/tpj.2013.5

Table 2.

Summary of GWAS and replication analyses in all asthma clinical trials.


Replication #1 Replication #2

SNP Chr MA MAF Gene Model CAMP GWAS (effect estimate) Pooled AT/LOCCS/LODO ACRN CARE GACRS Liptak Combined P val
rs11252394 10 A 0.08 Additive 0.0099b (+) 1.21E-06 0.4173 0.3472 - 1.98E-07
rs6988229 8 T 0.20 COL22A1 Recessive 0.0004c (+) 0.0050 0.0505 0.9283 0.0139 8.51E-06
rs9552679 13 C 0.26 Additive 0.0007d (−) 0.0004 0.7884 0.4410 - 3.02E-05
rs1663330 14 G 0.33 Additive 0.0020b (+) 0.0028 0.0234 0.7544 - 4.54E-05
rs1663332 14 T 0.37 Additive 0.0028b(+) 0.0006 0.0374 0.6874 0.3595 8.07E-05
rs17495520 5 T 0.14 Additive 0.038b (+) 0.0110 0.0030 0.3587 - 0.0003
rs10511905 9 G 0.22 Additive 0.006a (−) 0.0087 0.1388 0.3149 - 0.0003
rs518350 22 T 0.12 Recessive 0.0065e (+) 0.0010 0.4987 0.2090 0.3334 2.70E-04
rs17701271 4 A 0.22 Recessive 0.004c (+) 0.0026 0.1371 0.8756 0.2031 0.0003
rs6002674 22 C 0.15 Recessive 0.0012e (−) 0.0040 0.9808 0.0310 0.5675 0.0027
rs1419555 7 T 0.37 Additive 0.0043d (+) 0.0060 0.7723 0.6879 0.4932 0.0068
rs1423515 5 A 0.05 Additive 0.027b (+) 0.0400 0.4104 0.4710 - 0.0089
rs1522113 4 A 0.05 CLOCK Additive 0.014b (+) 0.0037 0.9260 0.0427 0.8633 0.0177

Association results for 13 replicated SNPs (p-values < 0.05) from the primary replication phase only are shown, sorted by Liptak Combined P-values. The p-values presented for CAMP are 2-sided while p-values for the replication populations are 1-sided, based on the direction of association (denoted as + or −) relative to the CAMP analysis. MAF: minor allele frequency in CAMP.

a

Lowest p-value is with the family-based association test (FBAT)

b

Lowest p-value is with the additive generalized linear model

c

Lowest p-value is with the recessive generalized linear model

d

Lowest p-value is with the additive longitudinal analysis

e

Lowest p-value is with the recessive longitudinal analysis