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Egyptian Journal of Medical Human Genetics

Table 6 Association between MDR1 C3435T SNP and epilepsy types (primary and secondary)

From: The association between MDR1 C3435T genetic polymorphism and the risk of multidrug-resistant epilepsy in Egyptian children

MDR1 C3435T genotype

Total cases, n = 106

Epilepsy type

χ2

p

OR (95%CI)

Primary, n = 72 (%)

Secondary, n = 34 (%)

CC(r)

50

35 (48.6)

15 (30.0)

  

1

CT

41

28 (38.9)

13 (31.7)

0.03

0.86

0.92 (0.38–2.26)

TT

15

9 (12.5)

6 (40.0)

0.53

0.5

0.6 (0.2–2.1)

  1. No statistically significant association was found between epileptic types (primary and secondary) and MDR1 C3435T genotype distribution
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