|
Analysis of the PTPN22 C1858T variant in the Spanish cohort |
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| Genotypes (%) |
Alleles (%) |
||||
| Subjects |
CC |
CT |
TT |
C |
T |
|
|
|||||
| Controls (n = 554) |
483 (87.2) |
68 (12.3) |
3 (0.5) |
1034 (93.3) |
74 (6.7) |
| Female (n = 197) |
172 (87.3) |
23 (11.7) |
2 (1.0) |
367 (93.1) |
27 (6.9) |
| Male (n = 189) |
168 (89.9) |
20 (10.6) |
1 (0.5) |
356 (94.2) |
22 (5.8) |
| Cases (n = 316) |
252 (79.7) |
59 (18.7) |
5 (1.6) |
563 (89.1) |
69 (10.9) |
| Female (n = 159) |
122 (76.7) |
33 (20.8) |
4 (2.5) |
277 (87.1) |
41 (12.9) |
| Male (n = 157) |
130 (82.8) |
26 (16.1) |
1 (0.6) |
286 (91.1) |
28 (8.9) |
|
Patients vs. controls: T vs. C; OR (95%) = 1.71 (1.20–2.45); p = 0.002 (TT+CT) vs. CC; OR (95%) = 1.73 (1.17–2.54); p = 0.004 | |||||
Santiago et al. BMC Medical Genetics 2007 8:54 doi:10.1186/1471-2350-8-54 |
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