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Table 1 Catechol-O-methyltransferase (COMT) genotype frequencies, allele frequencies and allele carriage in the total of 197 cancer patients

From: Genetic variation in the Catechol-O-Methyltransferase (COMT) gene and morphine requirements in cancer patients with pain

SNP (region)

Genotype

Genotype frequencies

Allele

Allele frequencies

Allele carriage

Rs2075507*

AA

0.26

A

0.53

0.80

(promoter)

AG

0.54

G

0.47

0.74

 

GG

0.20

   

Rs737866

AA

0.61

A

0.78

0.94

(intron 1)

AG

0.33

G

0.22

0.39

 

GG

0.06

   

Rs7287550

CC

0.53

C

0.72

0.91

(intron 1)

CT

0.38

T

0.28

0.47

 

TT

0.09

   

Rs5746849

GG

0.18

G

0.43

0.68

(intron 1)

GA

0.49

A

0.57

0.82

 

AA

0.33

   

Rs740603

AA

0.31

A

0.56

0.81

(intron 1)

AG

0.50

G

0.44

0.69

 

GG

0.19

   

Rs6269

AA

0.40

A

0.62

0.84

(intron 2)

AG

0.44

G

0.38

0.60

 

GG

0.16

   

Rs2239393

AA

0.40

A

0.62

0.84

(intron 3)

AG

0.44

G

0.38

0.59

 

GG

0.16

   

Rs4818

CC

0.41

C

0.63

0.84

(exon 4)

CG

0.43

G

0.37

0.59

 

GG

0.16

   

Rs4680 (Val158Met)

GG

0.22

G

0.44

0.66

(exon 4)

GA

0.44

A

0.56

0.78

 

AA

0.34

   

Rs174699

CT

0.09

C

0.04

0.09

(intron 5)

TT

0.91

T

0.96

100.0

Rs165728

CT

0.10

C

0.05

0.10

(untranslated region)

TT

0.90

T

0.95

100.0

  1. * Rs2075507 has recently been revised, earlier SNP number was Rs2097603