Skip to main content

Table 2 The allele frequency of 16 SNPs covering HSPG2

From: Rare variant of HSPG2 is not involved in the development of adolescent idiopathic scoliosis: evidence from a large-scale replication study

SNP

MA

MAF

p

OR (95% CI)

Patients (n = 1446)

Controls (n = 2080)

rs4654770

T

0.170

0.169

0.9262

1.01 (0.90–1.12)

rs12040859

T

0.190

0.192

0.8902

0.99 (0.87–1.11)

rs17459139

T

0.165

0.167

0.8384

0.99 (0.87–1.11)

rs7556412

G

0.179

0.195

0.1463

0.90 (0.81–0.99)

rs12043008

G

0.179

0.175

0.7164

1.03 (0.92–1.14)

rs10799718

A

0.385

0.371

0.278

1.06 (0.94–1.17)

rs11810496

G

0.393

0.390

0.8497

1.01 (0.90–1.12)

rs2445142

G

0.395

0.381

0.3187

1.06 (0.94–1.17)

rs878949

T

0.148

0.151

0.8051

0.99 (0.87–1.11)

rs2501257

A

0.395

0.386

0.5053

1.04 (0.94–1.16)

rs6680566

C

0.394

0.388

0.6465

1.03 (0.92–1.14)

rs6698486

G

0.347

0.341

0.6487

1.03 (0.92–1.14)

rs9426783

C

0.443

0.436

0.62

1.03 (0.92–1.14)

rs4654773

T

0.440

0.433

0.5781

1.03 (0.92–1.14)

rs16826053

C

0.199

0.189

0.383

1.06 (0.94–1.17)

rs10917067

T

0.107

0.116

0.2869

0.91 (0.82–1.01)

  1. MA indicates minor allele, MAF indicates minor allele frequency, OR indicates odds ratio, CI indicates confidential interval