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Table 2 Summary results of associations between 17 potentially functional SNPs in three genes (KCTD10, MVK and MMAB) and risk of dyslipidemia

From: Association of KCTD10, MVK, and MMAB polymorphisms with dyslipidemia and coronary heart disease in Han Chinese population

Gene

SNP

Allelea

Casesb

Controlsb

MAF

HWEc

Codominant modeld

Additive modeld

(N = 399)

(N = 465)

(Cases/controls)

P het

P hom

P add

KCTD10

rs1477117

G/A

279/115/1

326/123/10

0.148/0.156

0.686

0.349

0.025

0.791

rs11066782

C/T

283/113/1

311/135/11

0.145/0.172

0.414

0.929

0.014

0.174

rs11613718

C/T

272/120/1

308/139/9

0.155/0.172

0.138

0.762

0.038

0.521

rs11615336

C/A

282/101/1

317/120/10

0.134/0.157

0.730

0.931

0.024

0.288

rs7295954

C/T

322/60/1

381/69/0

0.081/0.077

0.078

0.399

0.323

rs1045582

G/T

284/104/2

321/124/6

0.138/0.151

0.118

0.888

0.112

0.459

MVK

rs3759387

G/T

297/97/3

330/126/7

0.130/0.151

0.194

0.990

0.303

0.687

rs2287218

C/T

279/112/4

324/122/10

0.152/0.156

0.707

0.494

0.095

0.878

MMAB

rs12817689

A/G

284/105/3

319/113/10

0.142/0.150

0.998

0.614

0.047

0.635

rs2241201

C/G

238/138/11

288/148/21

0.207/0.208

0.722

0.358

0.268

0.928

rs877710

C/G

194/177/26

219/201/40

0.288/0.305

0.522

0.656

0.330

0.714

rs11067233

C/G

315/74/2

329/118/8

0.100/0.147

0.486

0.072

0.145

0.026

rs9593

A/T

187/162/26

212/196/39

0.285/0.306

0.506

0.958

0.333

0.539

rs11067227

C/T

316/67/2

333/104/7

0.092/0.133

0.729

0.116

0.295

0.065

rs7134594

C/T

187/178/26

213/196/40

0.294/0.307

0.286

0.786

0.364

0.665

rs11831226

A/C

320/58/2

391/71/0

0.082/0.077

0.074

0.491

0.342

rs8228

A/G

322/63/0

380/69/0

0.082/0.077

0.078

0.349

0.349

  1. MAF minor allele frequency
  2. aMajor/minor allele
  3. bMajor homozygote/heterozygote/rare homozygote
  4. cHardy-Weinberg equilibrium test among controls
  5. dLogistic regression with adjustment for sex, age, smoking and BMI were used to test associations in codominant (P het: heterozygote vs. major homozygote; P hom: minor homozygote vs. major homozygote) and additive (P add: minor homozygote vs. heterozygote vs. major homozygote) models