Table 5.
Marker | χ25-a | pValue5-b | Susceptibility allele | Mode5-c |
---|---|---|---|---|
D1Mit235 | 12.6 | 0.002 | D2 | A |
D1Mit7 | 42.9 | 10−9 | D2 | D |
D1Mit11 | 48.1 | 10−9 | D2 | A |
D1Mit54 | 36.8 | 10−7 | D2 | A |
D1Mit30 | 41.7 | 10−9 | D2 | A |
D1Mit16 | 22.3 | 10−4 | D2 | A |
D1Mit150 | 36.2 | 10−7 | D2 | A |
D1Mit17 | 18.8 | 10−4 | D2 | A |
D3Mit268 | 11.6 | 0.003 | B6 | D |
D5Mit11 | 13.2 | 10−3 | B6 | R |
D5Mit15 | 10.2 | 0.006 | B6 | R |
D5Mit398 | 14.1 | 10−3 | B6 | R |
D5Mit95 | 11.6 | 0.003 | B6 | R |
D6Mit102 | 9.9 | 0.007 | D2 | D |
D6Mit55 | 7.6 | 0.02 | D2 | D |
D6Mit59 | 9.0 | 0.01 | D2 | D |
D18Mit49 | 8.4 | 0.015 | D2 | D |
Represents the association between genotype and seizure status based on the presence (n = 335) or absence (n = 176) of a PTZ-induced tonic-clonic seizure.
Only markers attaining a p < 0.02 threshold are shown.
Mode of inheritance was determined by best-fit regression analysis following marker recoding with seizure status as the dependent variable (D, dominant; R, recessive; A, additive).