Table 4

 Cx36 haplotype frequency in JME cases and controls

Haplotype*15q14 JME†, n (%)RS JME, n (%)Combined, n (%)Control, n (%)
*Haplotype inferred using PHASE for the four SNPs 333, 369, 588, and 888, respectively; p = 0.02 (p value computed using Fisher’s exact test, gives the significance value of the comparison of haplotype frequencies between JME and control cases).
ACCG13 (22.4)81 (28.9)94 (27.8)81 (32.9)
TCCG18 (31.1)82 (29.3)100 (29.6)79 (32.2)
TCTG16 (27.6)65 (23.2)81 (24)41 (16.7)
TCTA7 (12.1)32 (11.4)39 (11.5)28 (11.4)
TTCG1 (1.7)20 (7.2)21 (6.2)16 (6.5)
ACTG1 (1.7)01 (0.3)1 (0.3)
TTCA1 (1.7)01 (0.3)0
TCCA1 (1.7)01 (0.3)0