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Table 2 Frequency of mutant alleles among study subjects

From: Association of inherited thrombophilia mutations and their combinations among palestinian women with unexplained recurrent miscarriage

Mutation

Mutant allele frequency (%)

P-value

Patients

Controls

FVL R506Q

21

18

0.593

FII G20210A

1

3

0.314

MTHFR C677T

59

70

0.104

MTHFR A1298C

80

57

< 0.001

BFG − 455G > A

54

44

0.158

PAI1 5G/4G

78

88

0.060

FXIIIA V34L

33

17

0.009

FV HR2 H1299R

17

19

0.714

  1. Data are expressed as alleles where normal genotype was represented by zero alleles and hetro and homo mutants were represented by one and two alleles, respectively. Total no. of alleles was calculated by multiplying the number of alleles by the number of patients or controls. Data was analysis by the N-1 chi-square test and a p value < 0.05 was considered significant. The p-value in bold font was used to stress the significant values or values less than 0.05.
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Thrombosis Journal

ISSN: 1477-9560

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