SNP | Genotypes | AT (n=18) | No thyroid impairment (n=62) |
---|---|---|---|
C1858T | CC | 12 (66.7%) | 49 (79.0%) |
CT | 6 (33.3%) | 12 (19.4%) | |
TT | 0 (0.0%) | 1 (1.6%) | |
p=0.41034 | |||
A49G | AA | 7 (38.9%) | 26 (41.9%) |
AG | 11 (61.1%) | 36 (58.1%) | |
GG | 0 (0.0%) | 0 (0.0%) | |
p=0.81720 | |||
C(−318)T | CC | 14 (77.8%) | 47 (75.8%) |
CT | 4 (22.2%) | 13 (21.0%) | |
TT | 0 (0.0%) | 2 (3.2%) | |
p=0.74153 |