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Table 3 Warfarin pharmacogenetic profile obtained in the fifty-eight individuals, carriers of at least one variation in F5 or F2 genes and one in MTHFR

From: Thrombotic genetic risk factors and warfarin pharmacogenetic variants in São Miguel's healthy population (Azores)

 

Thrombotic risk factors

Warfarin pharmacogenetics

 

F5

F2

MTHFR

 

CYP2C9

 

VKORC1

N (%)

1691G>A

20210G>A

677C>T

1298A>C

430C>T

1075A>C

1639G>A

1 (1.7)

G A

GG

TT

AA

TT

A C

G A

1 (1.7)

G A

GG

TT

AA

C T

A C

AA

1 (1.7)

GA

GG

CC

AC

CT

AC

GA

2 (3.5)

GA

GG

CT

AA

CT

AC

GA

1 (1.7)

GA

GG

CC

AC

CT

AC

GG

1 (1.7)

GG

GA

CT

AC

CC

AC

AA

1 (1.7)

GA

GG

CC

CC

CC

AC

GA

1 (1.7)

GA

GG

CT

AC

CC

AC

GA

1 (1.7)

GG

G A

TT

AA

CC

A C

G A

1 (1.7)

GA

GG

CC

AC

CC

AC

GG

2 (3.5)

GA

GG

CT

AA

CC

AC

GG

1 (1.7)

G A

GG

TT

CC

TT

AA

G A

1 (1.7)

GA

GG

CT

AA

CT

AA

AA

1 (1.7)

GA

GG

CT

AC

CT

AA

GA

1 (1.7)

G A

GG

TT

AA

C T

AA

G A

2 (3.5)

GG

GA

CT

AC

CT

AA

GA

1 (1.7)

GG

GA

CT

AA

CT

AA

GG

2 (3.5)

GA

GG

CT

AA

CT

AA

GG

1 (1.7)

G A

GG

TT

AA

C T

AA

GG

2 (3.5)

GA

GG

CC

AC

CC

AA

AA

1 (1.7)

GA

GG

CT

AA

CC

AA

AA

3 (5.2)

G A

GG

TT

AA

CC

AA

AA

1 (1.7)

GG

GA

CC

AC

CC

AA

AA

1 (1.7)

GG

GA

CT

AC

CC

AA

AA

1 (1.7)

GG

G A

TT

AA

CC

AA

AA

2 (3.5)

GA

GG

CC

AC

CC

AA

GA

1 (1.7)

GA

GG

CT

AA

CC

AA

GA

2 (3.5)

GA

GG

CT

AC

CC

AA

GA

4 (6.9)

G A

GG

TT

AA

CC

AA

G A

1 (1.7)

GG

AA

CC

AC

CC

AA

GA

1 (1.7)

GG

GA

CC

AC

CC

AA

GA

1 (1.7)

GG

GA

CC

CC

CC

AA

GA

2 (3.5)

GG

GA

CT

AA

CC

AA

GA

2 (3.5)

GA

GG

CC

AC

CC

AA

GG

3 (5.2)

GA

GG

CT

AA

CC

AA

GG

2 (3.5)

GA

GG

CT

AC

CC

AA

GG

1 (1.7)

GG

GA

CC

CC

CC

AA

GG

1 (1.7)

GG

GA

CT

AA

CC

AA

GG

3 (5.2)

G A

GG

TT

AA

CC

AA

GG

  1. Italic characters indicate nucleotide changes considering the wild-type allele and in bold illustrate carriers of the F5 G1691A or F2 G20210A with MTHFR 677TT genotype conferring high thrombotic risk.