Table 2 Genotype distribution of the human SBF1 (GCC) repeat in the NCD and control groups.

From: A (GCC) repeat in SBF1 reveals a novel biological phenomenon in human and links to late onset neurocognitive disorder

Genotypes * Group Crosstabulation

 

Groupsa

Total

Controls

NCDs

Genotypes

5/6

 Count

0

1

1

 %

0.0%

0.4%

0.2%

6/8

 Count

12

11

23

 %

4.3%

4.2%

4.2%

6/9

 Count

4

0

4

 %

1.4%

0.0%

0.7%

7/8

 Count

1

0

1

 %

0.4%

0.0%

0.2%

8/8

 Count

93

100

193

 %

33.0%

38.5%

35.6%

8/9

 Count

23

45

68

 %

8.2%

17.3%

12.5%

8/10

 Count

2

0

2

 %

0.7%

0.0%

0.4%

9/9

 Count

141

101

242

 %

50.0%

38.8%

44.6%

9/10

 Count

4

1

5

 %

1.4%

0.4%

0.9%

10/10

 Count

2

1

3

 %

0.7%

0.4%

0.6%

Total

 Count

282

260

542

 %

100.0%

100.0%

100.0%

  1. aFisher’s exact p = 0.001. Counts and % represent within each group.