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Table 1 Genotypes and allele frequencies.

From: NPAS2 and PER2 are linked to risk factors of the metabolic syndrome

Gene

SNPa

Mutation Type

Allele 1b

Allele 2

n 1 (freq)C

n 2 (freq)

n 11 (freq)

n12 (freq)

n 22 (freq)

Acads

rs1799958

missense

G

A

768 (0.74)

266 (0.26)

283 (0.55)

202 (0.39)

32 (0.06)

Ada

22G>A

missense

G

A

978 (0.95)

56 (0.05)

461 (0.89)

56 (0.11)

0

Adcyap1

rs2856966

missense

A

G

850 (0.82)

184 (0.18)

344 (0.67)

162 (0.31)

11 (0.02)

Arntl

rs6486120

intronic

G

T

744 (0.72)

290 (0.28)

280 (0.54)

184 (0.36)

53 (0.10)

 

rs1982350

intronic

G

A

587 (0.57)

447 (0.43)

181 (0.35)

225 (0.44)

111 (0.21)

 

rs3816360

intronic

C

T

552 (0.53)

482 (0.47)

152 (0.29)

248 (0.48)

117 (0.23)

 

rs2278749

intronic

C

T

823 (0.80)

211 (0.20)

328 (0.63)

167 (0.32)

22 (0.04)

 

rs2290035

intronic

A

T

595 (0.58)

439 (0.42)

175 (0.34)

245 (0.47)

97 (0.19)

Arntl2

rs7958822

intronic

G

A

560 (0.54)

474 (0.46)

147 (0.28)

266 (0.51)

104 (0.20)

 

rs4964057

intronic

T

G

601 (0.58)

433 (0.42)

178 (0.34)

245 (0.47)

94 (0.18)

 

rs1037921

missense

A

G

947 (0.92)

87 (0.08)

433 (0.84)

81 (0.16)

3 (0.01)

 

rs2306074

intronic

T

C

668 (0.65)

366 (0.35)

213 (0.41)

242 (0.47)

62 (0.12)

 

rs35878285

mis-sense

A

 

1034 (1.00)

 

517(1.00)

  

Clock

rs2412646

intronic

C

T

760 (0.74)

274 (0.26)

280 (0.54)

200 (0.39)

37 (0.07)

 

rs11240

intronic

C

G

696 (0.67)

338 (0.33)

227 (0.44)

242 (0.47)

48 (0.09)

 

rs2412648

intronic

T

G

654 (0.63)

380 (0.37)

210 (0.41)

234 (0.45)

73 (0.14)

 

rs3805151

intronic

T

C

613 (0.59)

421 (0.41)

183 (0.35)

247 (0.48)

87 (0.17)

Cry2

rs2863712

missense

T

 

1034 (1.00)

 

517(1.00)

  

Drd2

rs1800497

missense

G

A

838 (0.81)

196 (0.19)

336 (0.65)

166 (0.32)

15 (0.03)

 

rs6277

silent

G

A

542 (0.52)

492 (0.48)

141 (0.27)

260 (0.50)

116 (0.22)

Fdft1

rs11549147

missense

A

G

944 (0.91)

90 (0.09)

431 (0.83)

82 (0.16)

4 (0.01)

Glo1

rs2736654

missense

T

G

662 (0.64)

372 (0.36)

207 (0.40)

248 (0.48)

62 (0.12)

Opn4

rs1079610

missense

T

C

714 (0.69)

320 (0.31)

246 (0.48)

222 (0.43)

49 (0.09)

Ncoa3

rs6094752

missense

C

T

1003 (0.97)

31 (0.03)

486 (0.94)

31 (0.06)

0

 

rs2230782

missense

G

C

932 (0.9)

102 (0.1)

422 (0.82)

88 (0.17)

7 (0.01)

 

rs2230783

missense

T

 

1034 (1.00)

 

517(1.00)

  

Npas2

rs11541353

missense

C

T

859 (0.83)

175 (0.17)

358 (0.69)

143 (0.28)

16 (0.03)

 

rs2305160

missense

G

A

727 (0.7)

307 (0.3)

252 (0.49)

223 (0.43)

42 (0.08)

Npy

rs16139

missense

T

C

956 (0.92)

78 (0.08)

444 (0.86)

68 (0.13)

5 (0.01)

Per2

rs934945

missense

C

T

917 (0.89)

117 (0.11)

402 (0.78)

113 (0.22)

2 (0.004)

 

10870

intronic

A

G

854 (0.83)

180 (0.17)

350 (0.68)

154 (0.30)

13 (0.03)

 

rs2304672

UTR 5'

G

C

865 (0.84)

169 (0.16)

361 (0.70)

143 (0.28)

13 (0.03)

 

S662G

missense

T

 

1034 (1.00)

 

517(1.00)

  

Plcb4

rs6077510

missense

A

G

552 (0.53)

482 (0.47)

142 (0.27)

268 (0.52)

107 (0.21)

Timeless

rs2291739

missense

A

G

624 (0.6)

410 (0.4)

193 (0.37)

238 (0.46)

86 (0.17)

 

rs2291738

intronic

C

T

546 (0.53)

488 (0.47)

147 (0.28)

252 (0.49)

118 (0.23)

Vip

rs3823082

intronic

C

T

854 (0.83)

180 (0.17)

351 (0.68)

152 (0.29)

14 (0.03)

 

rs688136

UTR 3'

T

C

676 (0.65)

358 (0.35)

221 (0.43)

234 (0.45)

62 (0.12)

Vipr2

rs885863

UTR 3'

T

C

518 (0.50)

516 (0.50)

126 (0.24)

266 (0.51)

125 (0.24)

  1. a) dbSNP symbols http://www.ncbi.nlm.nih.gov/SNP
  2. b) Alleles extracted from HapMap http://www.HapMap.org
  3. c) Total number of alleles in study sample, frequencies in parenthesis.