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Table 1 PBX1 SNPs nominally associated with type 2 diabetes in French Caucasians.

From: Evaluating the association of common PBX1variants with type 2 diabetes

SNP

Alleleb

Chr Position (NCBI36)

Gene Region

n subjects

Allele 1 (%)

Allele 2 (%)

P

OR (95% CI)

rs10918027

A/G

162765790

5' upstream

T2D

1414

2128 (75)

700 (25)

0.040

1.14 (1.01–1.28)

    

NG

1567

2429 (78)

705 (22)

  

rs1338625

A/C

162780889

5' upstream

T2D

1420

2107 (74)

733 (26)

0.039

1.13 (1.01–1.27)

    

NG

1576

2411 (76)

741 (24)

  

rs6662567

C/T

162783473

5' upstream

T2D

1433

2140 (75)

726 (25)

0.040

1.13 (1.01–1.27)

    

NG

1574

2422 (77)

726 (23)

  

rs6426870

T/C

162790577

5' upstream

T2D

1396

2073 (74)

719 (26)

0.014

1.16 (1.03–1.31)

    

NG

1542

2375 (77)

709 (23)

  

rs2275558 (G21S) a

G/A

162795744

Exon 1

T2D

1427

2193 (77)

661 (23)

0.013

1.17 (1.03–1.32)

    

NG

1626

2584 (79)

668 (21)

  

rs2792248 a

A/G

162891886

Intron 2

T2D

1178

1814 (77)

542 (23)

0.004

1.21 (1.06–1.39)

    

NG

1442

2121 (74)

763 (26)

  
  1. a SNPs that showed evidence of association with T2D (P < 0.05) in the French samples of the 1q Consortium; b SNP alleles are shown as major/minor.