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Table 2 Allele and genotype frequencies, respectively absolute and percentage (in brackets), of the five SNPs of the SCN1A gene observed in 49 cases and 100 controls, tested by HRM

From: Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?

 

SNPs of the SCN1A gene

1748A > T

2656T > C

3199A > G

5771G > A

5864T > C

Cases (N = 49)

 Allele frequencies

A

98 (100%)

T

98 (100%)

A

65 (66.3%)

G

98 (100%)

T

98 (100%)

T

0 (0%)

C

0 (0%)

G

33 (33.7%)

A

0 (0%)

C

0 (0%)

 Genotype frequencies

A/A

49 (100%)

T/T

49 (100%)

A/A

22 (44%)

G/G

49 (100%)

T/T

49 (100%)

A/T

0 (0%)

T/C

0 (0%)

A/G

21 (44.7%)

G/A

0 (0%)

T/C

0 (0%)

T/T

C/C

G/G

A/A

C/C

0 (0%)

0 (0%)

6 (11.3%)

0 (0%)

0 (0%)

Controls (N = 100)

 Allele frequencies

A

200 (100%)

T

200 (100%)

A

123 (61.5%)

G

200 (100%)

T

200 (100%)

T

0 (0%)

C

0 (0%)

G

77 (38.5%)

A

0 (0%)

C

0 (0%)

 Genotype frequencies

A/A

100 (100%)

T/T

100 (100%)

A/A

42 (37.8%)

G/G

100 (100%)

T/T

100 (100%)

A/T

0 (0%)

T/C

0 (0%)

A/G

39 (47.4%)

G/A

0 (0%)

T/C

0 (0%)

T/T

0 (0%)

C/C

0 (0%)

G/G

19 (14.8%)

A/A

0 (0%)

C/C

0 (0%)