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. 2015 Jan 1;19(1):3–8. doi: 10.1089/gtmb.2014.0130

Table 2.

Distribution of Genotypes and Alleles

SNP Group n Genotypes p Alleles p OR [95% CI]
rs235913     A/A A/C C/C   A C    
  PACG 212 46 (21.7%) 123 (58.0%) 43 (20.3%) 0.037 215 (0.507) 209 (0.493) 0.017 1.366 [1.055–1.776]
  Control 255 39 (15.3%) 141 (55.3%) 75 (29.4%)   219 (0.429) 291 (0.571)    
rs183532     A/A A/G G/G   A G    
  PACG 212 13 (0.061) 75 (0.354) 124 (0.585) 0.024 101 (0.238) 323 (0.762) 0.008 1.541 [1.117–2.127]
  Control 255 6 (0.024) 74 (0.290) 175 (0.686)   86 (0.169) 424 (0.831)    
rs12076134     G/G G/T T/T   G T    
  PACG 212 10 (0.047) 74 (0.349) 128 (0.604) 0.800 94 (0.222) 330 (0.778) 0.527 0.905 [0.666–1.230]
  Control 255 15 (0.059) 92 (0.361) 148 (0.580)   122 (0.239) 388 (0.761)    
rs235875     A/A A/G G/G   A G    
  PACG 212 33 (0.156) 97 (0.458) 82 (0.387) 0.989 163 (0.384) 261 (0.616) 0.905 0.984 [0.755–1.282]
  Control 255 40 (0.157) 118 (0.463) 97 (0.380)   198 (0.388) 312 (0.612)    

Bold value indicates the frequency of the AATG and AATA haplotypes was significantly higher for PACG patients than for control subjects (both p<0.001).

SNP, single-nucleotide polymorphism.