Skip to main content
. 2010 Jun 24;128(3):293–302. doi: 10.1007/s00439-010-0850-3

Table 2.

Genotype distribution of CSF1R polymorphisms in asthmatics (BA) and normal subjects (NC) of the study subjects

Loci Position rsSNP Subject N (%) Co-dominant Dominant Recessive
C/C C/R R/R OR(95% CI) p p corr OR(95% CI) p p corr OR(95% CI) p p corr
+20511C>T Intron11 rs216144 NC 166 (63.4) 84 (32.1) 12 (4.6) 1.55 (1.19–2.00) 0.001 0.02 1.67 (1.22–2.28) 0.001 0.03 1.85 (0.94–3.65) 0.07 1
BA 236 (50.5) 195 (41.8) 36 (7.7)
+22693T>C Intron11 rs216140 NC 74 (28.2) 145 (55.3) 43 (16.4) 1.22 (0.98–1.51) 0.08 1 0.94 (0.67–1.32) 0.71 1 1.99 (1.34–2.95) 0.0006 0.01
BA 136 (29) 212 (45.2) 121 (25.8)

* Controlled for age (continuous value), sex (male = 0, female = 1), atopy status (non-atopy = 0, atopy = 1), and smoking status (non-smoker = 0, ex-smoker = 1, smoker = 2) as co-variables. The effective number of independent marker loci in CSF1R was calculated to correct for multiple testing, using the software SNPSpD (http://genepi.qimr.edu.au/general/daleN/SNPSpD) (Nyholt 2004). The number of independent marker loci in CSF1R was calculated as 4.5008 and 20.0301 in ht-block1 and ht-block2