Table 5 of Mookherjee, Mol Vis 2011; 17:2618-2627.

Table 5. Genotype frequency of SNP (rs10038177) showing association with POAG.



Genotype
Patient
subgroup		 Frequency
in patients
(n)		 Frequency
in controls
(n)

p-value
OR
(95% CI)		 Relative
risk
(95% CI)
TT POAG 0.47 (152) 0.53 (161) 0.129 - -
  HTG 0.39 (045)   0.009 0.559 (0.362–0.864) 0.655 (0.466–0.915)
  NON-HTG 0.52 (107)   0.748 - -
CT POAG 0.45 (145) 0.40 (121) 0.210 - -
  HTG 0.47 (054)   0.219 - -
  NON-HTG 0.44 (091)   0.365 -
CC POAG 0.08 (26) 0.07 (021) 0.596 - -
  HTG 0.14 (017)   0.014* 2.306 (1.180–4.508) 1.722 (1.077–2.487)
  NON-HTG 0.04 (009)   0.223 - -

*Significant observation. Comparison of the genotype frequencies of rs10038177 among 323 POAG (116 HTG cases and 207 non-HTG cases) patients and 303 controls revealed biased distribution for the CC genotype (p=0.014) portraying risk for HTG patient group.

Mookherjee, Mol Vis 2011; 17:2618-2627. http://www.molvis.org/molvis/v17/a283

©2011 Molecular Vision http://www.molvis.org/molvis/

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