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Table 1 List and information of 37 SNPs in the analyzed region on chromosome 20q11.22

From: Evaluation of sample size effect on the identification of haplotype blocks

No.

dbSNP ID

Position

No. of used samples

Minor allele frequency

P value (HWE test)

P value (association test)

Odds ratio

   

Control

Case

Control

Case

Overall

Control

Case

Overall

Allele

Genotype

 

A001

rs819135

32,311,428

357

362

0.40

0.34

0.37

0.32

0.30

0.18

0.03

0.08

1.27

A002

rs6088466

32,377,195

358

361

0.46

0.50

0.48

0.84

0.79

0.99

0.17

0.37

1.16

A003

rs1205336

32,389,997

358

367

0.36

0.35

0.36

0.47

0.81

0.50

0.85

0.93

1.02

A004

rs3746455

32,420,877

357

367

0.36

0.35

0.35

0.72

0.87

0.72

0.86

0.98

1.02

A005

rs6058029

32,433,304

352

367

0.35

0.35

0.35

0.44

0.87

0.51

0.94

0.90

1.01

A006

rs6087579

32,448,816

354

367

0.36

0.35

0.36

0.78

0.87

0.76

0.86

0.98

1.02

A007

rs6579165

32,458,376

357

359

0.36

0.36

0.36

0.72

0.71

0.61

0.98

1.00

1.00

A008

rs4911420

32,462,315

358

365

0.36

0.35

0.35

0.80

0.84

0.75

0.74

0.95

1.04

A009

rs4277599

32,472,566

356

360

0.36

0.35

0.35

0.70

0.74

0.61

0.79

0.96

1.03

A010

rs2424992

32,475,721

354

366

0.36

0.35

0.35

0.67

0.80

0.63

0.85

0.97

1.02

A011

rs6120644

32,487,471

355

364

0.36

0.36

0.36

0.92

0.81

0.81

0.94

0.99

1.01

A012

rs3736762

32,500,997

357

361

0.36

0.36

0.36

0.72

0.87

0.71

0.96

0.99

1.01

A013

rs6059850

32,508,445

352

364

0.36

0.35

0.35

0.98

0.70

0.77

0.76

0.92

1.03

A014

rs6059856

32,521,615

355

367

0.36

0.35

0.36

0.92

0.87

0.85

0.85

0.98

1.02

A015

rs6059866

32,539,471

355

360

0.36

0.35

0.35

0.92

0.92

0.89

0.80

0.97

1.03

A016

rs6059868

32,543,121

357

366

0.36

0.35

0.35

0.72

0.91

0.75

0.85

0.97

1.02

A017

rs6088512

32,559,552

355

365

0.36

0.35

0.36

0.86

0.83

0.78

0.86

0.98

1.02

A018

rs6120669

32,568,689

356

367

0.36

0.35

0.36

0.88

0.87

0.83

0.83

0.98

1.02

A019

rs1122174

32,574,507

356

367

0.18

0.15

0.16

0.41

0.97

0.51

0.09

0.22

1.27

A020

rs6087592

32,578,164

353

367

0.35

0.36

0.35

0.66

0.96

0.79

0.87

0.92

1.02

A021

rs11167239

32,604,133

354

363

0.36

0.36

0.36

0.88

0.72

0.72

0.85

0.97

1.02

A022

rs6088527

32,619,502

354

361

0.36

0.35

0.36

0.90

0.48

0.56

0.83

0.90

1.02

A023

rs764597

32,624,886

357

365

0.36

0.36

0.36

0.89

0.65

0.67

0.92

0.97

1.01

A024

rs2889849

32,627,938

352

365

0.18

0.15

0.16

0.32

0.41

0.80

0.11

0.13

1.26

A025

rs932542

32,635,029

357

367

0.18

0.15

0.16

0.45

0.42

0.94

0.15

0.19

1.23

A026

rs2295444

32,637,544

354

360

0.36

0.35

0.36

0.93

0.47

0.65

0.73

0.80

1.04

A027

rs2378199

32,650,141

358

360

0.17

0.14

0.16

0.26

0.36

0.73

0.07

0.08

1.30

A028

rs6088536

32,652,767

358

359

0.36

0.36

0.36

0.97

0.65

0.77

0.88

0.93

1.02

A029

rs6141488

32,656,407

356

367

0.46

0.49

0.48

0.24

0.71

0.56

0.24

0.28

1.13

A030

rs6142210

32,686,673

355

361

0.46

0.49

0.48

0.26

0.56

0.70

0.28

0.27

1.12

A031

rs6088552

32,690,152

358

366

0.46

0.49

0.48

0.24

0.60

0.64

0.22

0.23

1.14

A032

rs7269596

32,692,724

352

365

0.47

0.50

0.48

0.27

0.64

0.65

0.26

0.29

1.13

A033

rs6087612

32,694,483

352

367

0.46

0.50

0.48

0.29

0.64

0.67

0.16

0.21

1.16

A034

rs4911158

32,703,173

357

363

0.46

0.50

0.48

0.31

0.56

0.74

0.18

0.22

1.15

A035

rs6087616

32,726,694

356

364

0.46

0.50

0.48

0.46

0.60

0.86

0.18

0.28

1.15

A036

rs1321306

32,730,040

353

365

0.46

0.49

0.48

0.22

0.71

0.54

0.23

0.26

1.13

A037

rs910870

32,756,554

355

360

0.25

0.23

0.24

0.56

0.64

0.93

0.31

0.45

1.13

  1. Genome position is based on the NCBI build 35. The number of called sample is the number after excluding the undetermined sample(s) with TaqMan assay. HWE denotes Hardy-Weinberg equilibrium. 95% CI denotes 95% confidence interval. The crude odds ratio was calculated for the allele model.