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Table 2 Characteristics of the 52 Single Nucleotide Polymorphisms (SNPs)

From: An association analysis to identify genetic variants linked to asthma and rhino-conjunctivitis in a cohort of Sicilian children

Chr

Gene

SNP name

QC

Alleles (M/m)

MAF

HWE p values

Missing (%)

GENO (AA/Aa/aa)

1

SELE

rs5361

T/G

9.9

0.005

5.4

814/161/18

2

ORMDL1

rs5742940

G/A

1.8

0.028

1.0

1004/33/2

3

CACNA2D2

rs12488468

LCR

G/T

48.2

0.014

25.9

187/432/159

3

DOCK3

rs76699816

HWEd

G/A

11.6

< 0.001

8.7

779/138/42

4

TLR1

rs17616434

T/C

47.1

0.020

5.6

295/459/237

4

TLR1

rs2101521

HWEd/LCR

G/A

34.4

< 0.001

15.6

444/274/168

4

TLR1

rs4833095

HWEd

T/C

48.4

< 0.001

7.1

292/422/261

4

TLR1

rs5743595

HWEd

A/G

30.5

< 0.001

5.8

506/363/120

4

TLR10

rs10004195

HWEd/LCR

T/A

46.2

< 0.001

11.0

309/387/238

4

TLR10

rs4274855

LCR

C/T

29.4

1.000

22.5

408/334/72

4

TLR2

rs11736691

GF

100.0

4

TLR6

rs1039560

T/C

33.4

0.126

3.3

455/442/118

4

TLR6

rs5743789

HWEd/LCR

A/T

29.5

< 0.001

19.8

460/268/114

5

IL13

rs1800925

C/T

18.4

0.721

4.6

668/300/34

5

IL13

rs1881457

A/C

18.4

0.720

2.8

681/305/35

5

IL13

rs20541

HWEd

G/A

14.5

< 0.001

7.1

734/200/41

6

IL17

rs7741835

C/T

19.4

0.371

5.0

659/291/48

9

DMRT1

rs3812523

A/G

15.6

0.074

3.4

733/245/36

9

IL33

rs1342326

A/C

21.8

0.174

3.5

627/331/55

9

IL33

rs928413

A/G

30.8

0.397

4.3

486/418/101

11

ANO9

rs7482596

HWEd

G/T

13.3

< 0.001

4.2

770/205/31

11

ANO9

rs7484182

HWEd

T/C

14.1

< 0.001

4.1

758/215/34

11

DHCR7

rs1044482

GF

100.0

11

GST-P1

rs1695

HWEd

A/G

29.9

< 0.001

6.2

521/338/126

11

NADSYN1

rs2186777

A/C

26.7

0.014

4.5

553/365/85

11

SIGIRR

rs4074794

HWEd

G/A

19.5

< 0.001

6.3

659/266/59

12

IRAK3

rs1152918

C/T

6.9

0.295

2.1

893/128/7

12

IRAK3

rs2701652

G/C

22.0

0.256

4.1

620/330/57

12

ORMDL2

rs7954619

GF

100.0

16

IL4R

rs1801275

A/G

16.0

0.001

4.7

722/237/42

16

IL4R

rs1805012

HWEd

T/C

5.8

< 0.001

2.6

916/96/11

16

IL4R

rs3024548

HWEd/LCR

C/G

46.4

< 0.001

13.0

314/351/249

17

ERBB2

rs1058808

G/C

30.6

0.009

6.8

495/369/115

17

ERBB2

rs1136201

HWEd

A/G

13.8

< 0.001

4.1

767/203/37

17

ERBB2

rs2934971

GF

100.0

17

ERBB2

rs2952155

GF

100.0

17

ERBB2

rs4252665

C/T

1.7

0.137

1.6

999/33/1

17

GSDMA

rs3859192

C/T

37.9

0.028

6.5

398/423/161

17

GSDMA

rs3894194

G/A

41.6

0.005

5.3

359/442/193

17

GSDMA

rs7212938

T/G

44.2

0.039

4.8

326/463/211

17

GSDMB

rs2305479

C/T

42.0

0.166

1.9

355/485/190

17

GSDMB

rs2305480

G/A

40.2

0.088

3.8

371/466/173

17

GSDMB

rs7216389

HWEd

T/C

42.2

< 0.001

6.6

359/416/206

17

LRRC3C

rs8065126

HWEd/LCR

C/T

38.3

< 0.001

12.5

386/362/171

17

LRRC3C

rs8079416

T/C

45.2

0.013

4.5

315/469/219

17

MAP2K3

rs10468608

HWEd/LCR

C/T

30.2

< 0.001

19.8

462/251/129

17

MAP2K3

rs2363226

GF

100.0

17

MAP2K4

rs3760201

HWEd/LCR

A/G

32.9

< 0.001

34.6

343/236/108

17

ORMDL3

rs8076131

HWEd/LCR

A/G

40.7

< 0.001

15.9

333/382/168

17

PGAP3

rs1495102

HWEd/LCR

C/T

14.0

< 0.001

17.7

697/92/75

17

ZPBP2

rs11557467

GF

100.0

X

IRAK1

rs1059703

HWEd

A/G

25.5

< 0.001

4.2

679/140/187

  1. Chr chromosome, MAF minor allele frequency, GF genotyping failing, LCR low call rate, HWEd deviation from the Hardy-Weinberg equilibrium; A: major allele; a: minor allele; bold values indicate significance (p-values < 0.001)