Table 1. Genotype and allele frequencies for GRIN2A_rs4998386 in Parkinson's disease case/control in southeastern Swedish population.
| Genotype counts (%) | Allele frequency (%) | |||||||||
| N | CC | TC | TT | OR(95% CI) | pa | C | T | OR(95% CI) | pa | |
| PD | 193 | 159 (82.0) | 30 (16.0) | 4 (2.0) | 0.65(0.42–1.01)c | 0.06c | 348 (90.1) | 38b (9.9) | 0.73(0.49–1.09)b | 0.12b |
| - | - | - | - | 0.61(0.39–0.96)d | 0.03d | 348 (92.0) | 30d (8.0) | 0.64(0.42–0.99)d | 0.04d d d | |
| Control | 377 | 284 (75.3) | 88 (23.3) | 5 (1.3) | - | - | 656 (87.0) | 98b (13.0) | - | - |
| - | - | - | - | - | - | 656 (88.2) | 88d (11.8) | - | - | |
a
P-value: Chi-square test.
b
Including rare TT genotype.
c
Dominant model. Wild type CC vs. T carrier (TC+TT).
d
Excluding rare TT genotype.