Table 1

Information of genotyped SNPs

Gene

Order

SNP ID

Location from transcription site

Nucleotide variation

Rarer allele frequency

COMT

1

rs5746846

-8,663

G/C

0.43

2

rs2020917

-425

C/T

0.29

3

rs933271

2,099

T/C

0.29

4

rs5993882

8,225

T/G

0.25

5

rs740603

15,869

G/A

0.43

6

rs4646312

19,029

T/C

0.40

7

rs165722

19,705

T/C

0.45

8

rs6269

20,644

A/G

0.40

9

rs4633

20,927

T/C

0.46

10

rs4818

21,899

C/G

0.41

11

rs4680

21,963

A/G

0.46

12

rs174699

25,150

T/C

0.03

13

rs165728

27,715

T/C

0.04

MAOA

1

rs3788862

1,956

A/G

0.34

2

rs909525

37,794

T/C

0.38

3

rs2283274

44,168

A/G

0.38

4

rs1800659

58,761

A/G

0.33

5

rs979606

85,734

T/C

0.33

6

rs979605

85,955

G/A

0.33

7

87,983

C/T

0.34

8

rs2064070

93,274

T/A

0.36

MAOB

1

rs2283729

63,640

C/T

0.28

2

rs3027452

83,893

C/T

0.20

3

rs1799836

113,683

G/A

0.47

SLC6A2

1

7,551

C/T

0.06

2

rs40434

8,968

A/G

0.41

3

rs36017

28,261

G/C

0.49

SLC6A3

1

rs6350

2,347

C/T

0.09

2

rs403636

7,192

G/T

0.14

3

rs40184

50,469

G/A

0.41

4

rs12516948

54,177

T/C

0.35

5

rs10064219

60,548

C/T

0.14

SLC6A4

1

rs2066713

10,852

C/T

0.38

2

22,674

G/A

0.01

3

rs140701

24,184

G/A

0.45

4

rs4325622

36,247

A/G

0.49

5

rs1979572

50,741

C/T

0.48

DRD2

1

rs12421616

8,105

G/A

0.12

2

rs4322431

12,929

A/T

0.26

3

rs4581480

21,411

A/G

0.13

4

rs4936272

26,977

G/A

0.46

5

rs4648318

32,495

A/G

0.29

6

rs11608185

51,187

G/A

0.49

7

rs2734837

59,336

A/G

0.47

8

rs6277

62,706

T/C

0.46

9

rs6279

65,092

G/C

0.28

Kim et al. Molecular Pain 2006 2:24   doi:10.1186/1744-8069-2-24