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. 2011 Apr 1;13(4):243–248.

Table 4: Genotype and allele frequencies in patients and healthy people.

SNP Control Patient P-value
N % N %
TNF-238 Genotype NSa
G/G 98 95.1 84 90.3
G/A 5 4.9 9 9.7
A/A 0 - 0 -
Allele frequency NS
G 201 97.6 177 95.2
A 5 2.4 9 4.8
TNF-244 Genotype NS
G/G 103 100 93 100
G/A 0 - 0 -
A/A 0 - 0 -
Allele frequency NS
G 206 100 186 100
A - 0 - 0
TNF-308 Genotype NS
G/G 87 84.5 84 90.3
G/A 16 15.5 9 9.7
A/A 0 - 0 -
Allele frequency NS
G 190 92.2 177 95.2
A 16 7.8 9 4.8
TNF-857 Genotype 0.001
C/C 83 80.6 51 54.8
C/T 18 17.5 42 45.2
T/T 2 1.9 0 -
Allele frequency 0.002b
C 184 89.3 144 77.4
T 22 10.7 42 22.6
TNF-863 Genotype NS
C/C 74 71.8 69 74.2
C/A 29 28.2 21 22.6
A/A 0 - 3 3.2
Allele frequency NS
C 177 85.9 159 85.5
A 29 14.1 27 14.5

a NS: Nonsignificant

b odds: 2.4, C.I 95% (1.3-4.4)